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Genomic copy number variation in disorders of cognitive development
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
title
Genomic copy number variation in disorders of cognitive development
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
author
Eric M. Morrow
object named as
Eric M Morrow
series ordinal
1
0 references
publication date
1 November 2010
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
number of pages
14
1 reference
based on heuristic
inferred from page(s)
published in
Journal of the American Academy of Child and Adolescent Psychiatry
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
volume
49
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
page(s)
1091-1104
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
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Strong association of de novo copy number mutations with sporadic schizophrenia
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
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Structural variation of chromosomes in autism spectrum disorder
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Association between microdeletion and microduplication at 16p11.2 and autism
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Disruption of neurexin 1 associated with autism spectrum disorder
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Recurrent 16p11.2 microdeletions in autism
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When half is not enough: gene expression and dosage in the 22q11 deletion syndrome
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Genomic rearrangements and sporadic disease
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Strong association of de novo copy number mutations with autism
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Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation
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Copy number variation: new insights in genome diversity
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Structural variation of the human genome
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Musical behavior in a neurogenetic developmental disorder: evidence from Williams Syndrome.
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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
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9 July 2018
The molecular genetics of the 22q11-associated schizophrenia
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9 July 2018
Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.
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Eugen Bleuler's Concepts of Psychopathology
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I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses
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9 July 2018
Adoption studies of schizophrenia
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9 July 2018
Familial transmission of risk factors in the first-degree relatives of schizophrenic people
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22q11 deletion syndrome: a genetic subtype of schizophrenia
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'Pfropfschizophrenie' revisited. Schizophrenia in people with mild learning disability
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9 July 2018
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
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The prevalence of mental retardation: a critical review of recent literature.
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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.
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Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome
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9 July 2018
Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder
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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome
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9 July 2018
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
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Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
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27 September 2018
Genetic counseling for the 22q11.2 deletion.
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27 September 2018
The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
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Common deletion polymorphisms in the human genome.
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27 September 2018
Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment
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Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137887
retrieved
27 September 2018
Schizophrenia and chromosomal deletions within 22q11.2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137887
retrieved
27 September 2018
22q11 deletion syndrome in childhood onset schizophrenia: an update
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137887
retrieved
8 December 2018
Trisomy 15q25.2-qter in an autistic child: Genotype-phenotype correlations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20970697
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Lessons from childhood-onset schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20970697
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.JAAC.2010.08.009
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
PMCID
3137887
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
PubMed ID
20970697
1 reference
stated in
Europe PubMed Central
PubMed ID
20970697
retrieved
6 August 2017
ResearchGate publication ID
47533495
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