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Childhood autism and associated comorbidities
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Childhood autism and associated comorbidities
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
main subject
comorbidity
0 references
autism
0 references
author
Dimitrios I. Zafeiriou
series ordinal
1
object named as
Dimitrios I Zafeiriou
author given names
Dimitrios I
author last names
Zafeiriou
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
author name string
Athena Ververi
series ordinal
2
author given names
Athena
author last names
Ververi
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
Euthymia Vargiami
series ordinal
3
author given names
Euthymia
author last names
Vargiami
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
language of work or name
English
0 references
publication date
7 November 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
published in
Brain and Development
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
volume
29
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
page(s)
257-272
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
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Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism.
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PTEN mutation in a family with Cowden syndrome and autism
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Severe impairments of social interaction and associated abnormalities in children: Epidemiology and classification
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Autistic behaviors in a boy with Noonan syndrome.
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Autism, mental retardation, and chromosomal abnormalities
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Brief report: four case histories and a literature review of Williams syndrome and autistic behavior
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Williams syndrome: serotonin's association with developmental disabilities.
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Infantile autism and Duchenne muscular dystrophy.
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FISH-mapping of a 100-kb terminal 22q13 deletion
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The neurobeachin gene spans the common fragile site FRA13A.
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Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.
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Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.
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Behavioural characteristics and autistic features in individuals with Cohen Syndrome.
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Childhood onset neuropsychiatric disorders in adult eating disorder patients. A pilot study.
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The population prevalence of child psychiatric disorders in Danish 8- to 9-year-old children
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Specific Genetic Disorders and Autism: Clinical Contribution Towards their Identification
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7 January 2021
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Relative carnitine deficiency in autism
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Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome
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Autistic features in Joubert syndrome: a genetic disorder with agenesis of the cerebellar vermis
1 reference
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7 January 2021
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X chromosome and infantile autism.
1 reference
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7 January 2021
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Genes with triplet repeats: candidate mediators of neuropsychiatric disorders
1 reference
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7 January 2021
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Autism in Angelman syndrome: a population-based study
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Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications
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inferred from DOI database lookup
The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
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inferred from DOI database lookup
RNA binding proteins and the regulation of neuronal synaptic plasticity.
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autism in tuberous sclerosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal serotonergic development in a mouse model for the Smith-Lemli-Opitz syndrome: implications for autism
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal administration of thalidomide or valproic acid causes abnormal serotonergic neurons in the offspring: implication for pathogenesis of autism
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autism associated with conditions characterized by developmental errors in early embryogenesis: a mini review
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
X Chromosomal effects on social cognitive processing and emotion regulation: A study with Klinefelter men (47,XXY).
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Vasoactive intestinal peptide in the brain of a mouse model for Down syndrome
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autism associated with Williams syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
MMR vaccination and pervasive developmental disorders: a case-control study
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and macrocephaly.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
The sex chromosomes--one key to autism? An XYY case of infantile autism.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autism: a mitochondrial disorder?
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Serotonin and brain development: role in human developmental diseases
1 reference
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https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
A biogenic amine-synapse mechanism for mental retardation and developmental disabilities
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Does an imbalance between the dorsal and ventral striatopallidal systems play a role in Tourette's syndrome? A neuronal circuit approach
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomelanosis of ITO. A study of 76 infantile cases.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic anticipation. Expanding tandem repeats.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Gene structure and genetic localization of the PCLO gene encoding the presynaptic active zone protein Piccolo
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
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7 January 2021
based on heuristic
inferred from DOI database lookup
Basal ganglia dysfunction in Tourette's syndrome: a new hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile spasms in Down syndrome--effects of delayed anticonvulsive treatment.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mental and behavioural outcome of infantile epilepsy treated by vigabatrin in tuberous sclerosis patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical characteristics and diagnosis of Smith-Lemli-Opitz syndrome and tentative phenotype-genotype correlation: report of 45 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Duchenne muscular dystrophy population in Denmark, 1977-2001: prevalence, incidence and survival in relation to the introduction of ventilator use.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnosis and management of tuberous sclerosis complex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characteristics of fetal anticonvulsant syndrome associated autistic disorder.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autistic regression associated with seizure onset in an infant with tuberous sclerosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism as a strongly genetic disorder: evidence from a British twin study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: a large scale study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Metabolic approaches to the treatment of autism spectrum disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brief report: A case of autism with interstitial deletion of chromosome 13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two children with muscular dystrophies ascertained due to referral for diagnosis of autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and phenylketonuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of chromosome 2q37 and autism: a distinct subtype?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autistic behaviors among girls with fragile X syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autistic behavior in young boys with fragile X syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and tuberous sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Model of autism: increased ratio of excitation/inhibition in key neural systems
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haploinsufficiency of NSD1 causes Sotos syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Screening of the ARX gene in 682 retarded males.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurological and psychological findings in patients with Cohen syndrome: a study of 18 patients aged 11 months to 57 years
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Childhood Psychosis Combined with XYY Abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Growth during puberty in the XYY boy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protean PTEN: form and function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tourette syndrome, associated conditions and the complexities of treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuro-epileptic determinants of autism spectrum disorders in tuberous sclerosis complex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Perinatal risk factors for infantile autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Asperger's syndrome and ligamentous laxity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and Ehlers-Danlos syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent hypersomnia in two adolescent males with Asperger's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Childhood Autism in a female with Coffin Siris Syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lessons from fragile X regarding neurobiology, autism, and neurodegeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The first and second branchial arch syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropsychiatric disorders in the 22q11 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FMR1 and the fragile X syndrome: human genome epidemiology review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quasi-autistic patterns following severe early global privation. English and Romanian Adoptees (ERA) Study Team
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fetal gonadal histology in XXXXY, XYY and XXX syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism in Angelman syndrome: implications for autism research.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Joubert syndrome: review and report of seven new cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile autism: a genetic study of 21 twin pairs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and known medical conditions: myth and substance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No effect of MMR withdrawal on the incidence of autism: a total population study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropsychiatric assessment of children with autism: a population-based study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomelanosis of Ito in Three Cases with Autism and Autistic-like Conditions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and hypomelanosis of Ito in twins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism in thalidomide embryopathy: a population study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Asperger syndrome associated with Steinert's myotonic dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Attention deficits and autistic spectrum problems in children exposed to alcohol during gestation: a follow-up study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism in fetal alcohol syndrome: a report of six cases.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autistic behaviour in Moebius syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiology of tuberous sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioural phenotype of Cornelia de Lange syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype and psychological phenotype in tuberous sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioural phenotype of Bardet-Biedl syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Concordance for the syndrome of autism in 40 pairs of afflicted twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pervasive developmental disorders in preschool children: confirmation of high prevalence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and plumbism. A possible association
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overgrowth. Section V. Syndromes and other disorders associated with overgrowth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
47,XYY karyotypes and pervasive developmental disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Etiology and pathophysiology of autistic behavior: clues from two cases with an unusual variant of neuroaxonal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Should autistic children be evaluated for mitochondrial disorders?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and tuberous sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of Duchenne muscular dystrophy with autism spectrum disorder.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oromotor and communication findings in joubert syndrome: further evidence of multisystem apraxia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic susceptibility to neurodevelopmental disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and autistic behavior in Joubert syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Associated medical disorders and disabilities in children with autistic disorder: a population-based study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is Autism More Common Now than Ten Years Ago?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuroanatomy of fragile X syndrome: the temporal lobe
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cross-sectional area of the posterior hippocampus in autistic patients with cerebellar and corpus callosum abnormalities.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism and the environment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tracing the Origins of Autism: A Spectrum of New Studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autism spectrum disorders in relation to distribution of hazardous air pollutants in the san francisco bay area
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down syndrome: interaction between culture, demography, and biology in determining the prevalence of a genetic trait.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
45,X/46,XY mosaicism: report of 27 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
National Institutes of Health Consensus Development Conference Statement: phenylketonuria: screening and management, October 16-18, 2000.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Health supervision for children with Turner syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MMR vaccination and autism : what is the evidence for a causal association?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular Cytogenetics of Autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lead intoxication in children with pervasive developmental disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.BRAINDEV.2006.09.003
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/J.BRAINDEV.2006.09.003
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
PubMed ID
17084999
1 reference
stated in
Europe PubMed Central
PubMed ID
17084999
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17084999%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 December 2019
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