(Q34278925)

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The genetics of autism.

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Europe PubMed Central

PubMed publication ID

1 August 2017

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Europe PubMed Central

The genetics of autism. (English)

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Europe PubMed Central

PubMed publication ID

1 August 2017

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author name string

M Lauritsen

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

H Ewald

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

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publication date

1 June 2001

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Europe PubMed Central

PubMed publication ID

1 August 2017

Acta Psychiatrica Scandinavica

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Europe PubMed Central

PubMed publication ID

1 August 2017

103

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Europe PubMed Central

PubMed publication ID

1 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

411-427

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

The epidemiology of autism: a review.

1 reference

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21 January 2018

Autism: not an extremely rare disorder

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21 January 2018

Autism and known medical conditions: myth and substance

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21 January 2018

Epilepsy in autism and autisticlike conditions. A population-based study.

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21 January 2018

Mental retardation: genetic findings, clinical implications and research agenda

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https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism in children with congenital rubella

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21 January 2018

Autism and congenital cytomegalovirus

1 reference

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21 January 2018

RETRACTED: Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism diagnostic interview: a standardized investigator-based instrument.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

The incidence of cognitive disabilities in the siblings of autistic children.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Familial heterogeneity in infantile autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A case-control family history study of autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Stoppage rules and genetic studies of autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

The outcome in children with childhood autism and Asperger syndrome originally diagnosed as psychotic. A 30-year follow-up study of subjects hospitalized as children

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Concordance for the syndrome of autism in 40 pairs of afflicted twins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Infantile autism: a genetic study of 21 twin pairs

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A broader phenotype of autism: the clinical spectrum in twins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Cognitive assessment of siblings of autistic children.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A family study of autism: cognitive patterns and levels in parents and siblings.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Personality characteristics of parents of autistic children: a controlled study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Parents and collateral relatives of children with pervasive developmental disorders: a family history study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Variable expression of the autism broader phenotype: findings from extended pedigrees.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Identification of the phenotype in psychiatric genetics.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and genetics. A decade of research

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Male-to-male transmission in extended pedigrees with multiple cases of autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Genetic linkage and complex diseases, with special reference to psychiatric disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A genomic screen of autism: evidence for a multilocus etiology

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and genetic disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Chromosomal disorders and autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Chromosomal abnormalities in a series of children with autistic disorder.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism associated with marker chromosome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Maternal origin of inv dup(15) chromosomes in infantile autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism is not associated with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autistic behavior in young boys with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Fragile X syndrome, DSM-III-R, and autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

An analysis of autism in fifty males with the fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Brief report: screening children with autism for fragile-X syndrome and phenylketonuria.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Fragile X and autism: a multicenter survey.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Fragile X syndrome in a population of autistic children.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Fragile X syndrome in autistic boys.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

The fragile X marker and autism in perspective.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Prevalence of the fragile X anomaly amongst autistic twins and singletons.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Molecular and cytogenetic analyses of autism in Taiwan.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

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

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Early development, temperament, and functional impairment in autism and fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A prevalence study of autism in tuberous sclerosis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Association of tuberous sclerosis of temporal lobes with autism and atypical autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism in tuberous sclerosis complex.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and tuberous sclerosis complex: prevalence and clinical features

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism in tuberous sclerosis: evoked potential evidence for a deficit in auditory sensory processing.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

The treatment of epilepsy in autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Childhood psychosis and neurofibromatosis--more than a coincidence?

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Magnetic resonance imaging of high level autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Brief report: the association of neurofibromatosis type 1 and autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Candidate genes in psychiatry: an epidemiological perspective.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Associations of disease with genetic markers: déjà vu all over again.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Gene mapping studies with the syndrome of autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and the X chromosome. Multipoint sib-pair analysis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Lack of association between three genetic markers of brain growth factors and infantile autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Association study with two markers of a human homeogene in infantile autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Scanning of the dopamine D1 and D5 receptor genes by REF in neuropsychiatric patients reveals a novel missense change at a highly conserved amino acid

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Increased frequency of the null allele at the complement C4b locus in autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Increased frequency of the extended or ancestral haplotype B44-SC30-DR4 in autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

CD4+ helper T cell depression in autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Deficiency of suppressor-inducer (CD4+CD45RA+) T cells in autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Genetic studies of autistic disorder and chromosome 7

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Possible association of c-Harvey-Ras-1 (HRAS-1) marker with autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and genetics: clinical approach and association study with two markers of HRAS gene.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Serotonin transporter (5-HTT) gene variants associated with autism?

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Evidence of linkage between the serotonin transporter and autistic disorder.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A mutation in adenylosuccinate lyase associated with mental retardation and autistic features

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

X chromosome and infantile autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Hypomelanosis of ITO. A study of 76 infantile cases.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Hypomelanosis of Ito--report of four cases and survey of the literature.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism associated with Williams syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

"Autistic" behavior in two children with Williams-Beuren syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Brief report: four case histories and a literature review of Williams syndrome and autistic behavior

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Childhood psychosis in a case of Moebius syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autistic behaviour in Moebius syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autistic disorder in Sotos syndrome: a case report.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autistic features in Joubert syndrome: a genetic disorder with agenesis of the cerebellar vermis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autism and autistic behavior in Joubert syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Autistic disorders in children with CHARGE association.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

A Chinese classic phenylketonuria manifested as autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Phenylketonuria: an underlying etiology of autistic syndrome. A case report

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

21 January 2018

Psychometric assessment of first-degree relatives of 62 autistic probands in Utah

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Social language use in parents of autistic individuals

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of the fragile X syndrome in four birth cohorts of children of school age

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequency of the fragile X syndrome in infantile autism. A Swedish multicenter study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Autism and medical disorders: a review of the literature.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Epidemiology of tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Psychiatric disorder among children with tuberous sclerosis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Autism and tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Autistic behaviour and attention deficits in tuberous sclerosis: a population-based study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Strong association of the third hypervariable region of HLA-DR beta 1 with autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

The Dopamine D2 Receptor Locus as a Modifying Gene in Neuropsychiatric Disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

CGG repeat interruptions in the FMR1 gene in patients with infantile autism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

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

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Autism and hypomelanosis of Ito in twins.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

De novo purine synthesis is increased in the fibroblasts of purine autism patients.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0447.2001.00086.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1600-0447.2001.00086.X

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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