(Q34108364)

31 July 2017

1 reference

title

The molecular genetics of autism (English)

1 reference

31 July 2017

0 references

Wassink TH

1

1 reference

31 July 2017

Piven J

series ordinal

2

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 April 2000

1 reference

Current Psychiatry Reports

31 July 2017

published in

1 reference

31 July 2017

volume

2

1 reference

31 July 2017

issue

2

1 reference

31 July 2017

page(s)

170-175

1 reference

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

31 July 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11920-000-0063-X

New developments in the neurobiology of the tuberous sclerosis complex

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11920-000-0063-X

The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities

21 January 2018

1 reference

12 December 2020

Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome

1 reference

12 December 2020

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

1 reference

12 December 2020

The epidemiology of autism: a review.

1 reference

12 December 2020

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

1 reference

12 December 2020

Cognitive deficits in parents from multiple-incidence autism families

1 reference

12 December 2020

Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

1 reference

12 December 2020

Autism and tuberous sclerosis

1 reference

12 December 2020

Personality and language characteristics in parents from multiple-incidence autism families

1 reference

12 December 2020

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

12 December 2020

Genetics of autism: overview and new directions

1 reference

12 December 2020

Localisation of a gene implicated in a severe speech and language disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

An MRI study of the basal ganglia in autism

1 reference

12 December 2020

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

1 reference

12 December 2020

Mutation screening of the UBE3A/E6-AP gene in autistic disorder

1 reference

12 December 2020

Heterogeneity and the genetics of autism

1 reference

12 December 2020

Genetic studies of autistic disorder and chromosome 7

1 reference

12 December 2020

Infantile autism: a genetic study of 21 twin pairs

1 reference

12 December 2020

Masquerading repeats: paralogous pitfalls of the human genome

1 reference

12 December 2020

Executive function in parents of children with autism.

1 reference

12 December 2020

Autism and tuberous sclerosis complex: prevalence and clinical features

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex

1 reference

12 December 2020

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

12 December 2020

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

12 December 2020

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

1 reference

12 December 2020

An autosomal genomic screen for autism. Collaborative linkage study of autism

1 reference

12 December 2020

Xp deletions associated with autism in three females

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosomal disorders and autism

1 reference

12 December 2020

A case-control family history study of autism

1 reference

12 December 2020

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

12 December 2020

Biology of the fragile X mental retardation protein, an RNA-binding protein

1 reference

12 December 2020

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

12 December 2020

A genomic screen of autism: evidence for a multilocus etiology

1 reference

12 December 2020

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

1 reference

12 December 2020

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

1 reference

12 December 2020

Chromosomal abnormalities in a series of children with autistic disorder

1 reference

12 December 2020

Characterization of the cytosolic tuberin-hamartin complex. Tuberin is a cytosolic chaperone for hamartin

1 reference

12 December 2020

Association study of the NF1 gene and autistic disorder

1 reference

12 December 2020

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

12 December 2020

Autism: not an extremely rare disorder

1 reference

12 December 2020

A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications

1 reference

12 December 2020

Genetic studies in autistic disorder and chromosome 15.

1 reference

12 December 2020

10.1007/S11920-000-0063-X

Identifiers

DOI

1 reference

Dimensions Publication ID

31 July 2017

1026889400

0 references

1 reference