(Q35299131)

7 August 2017

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title

Molecular genetics of autism spectrum disorders (English)

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7 August 2017

autism spectrum disorder

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autism

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author name string

Barkur S Shastry

series ordinal

1

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7 August 2017

11 September 2003

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Journal of Human Genetics

7 August 2017

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7 August 2017

48

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7 August 2017

10

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7 August 2017

495-501

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https://scigraph.springernature.com/pub.10.1007/s10038-003-0064-9

7 August 2017

0 references

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Evaluation of FOXP2 as an autism susceptibility gene

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Partial 6p trisomy associated with infantile autism.

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

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A genomewide screen for autism susceptibility loci

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Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism

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12 December 2020

No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21‐q22 and autism

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12 December 2020

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

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12 December 2020

Presence of large deletions in kindreds with autism

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12 December 2020

FOXP2 is not a major susceptibility gene for autism or specific language impairment

1 reference

12 December 2020

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

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12 December 2020

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12 December 2020

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

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12 December 2020

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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12 December 2020

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12 December 2020

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

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12 December 2020

Medial temporal lobe structures and autism: a review of clinical and experimental findings.

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A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autism.

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

Investigation of two variants in the DOPA decarboxylase gene in patients with autism

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12 December 2020

Severe impairments of social interaction and associated abnormalities in children: Epidemiology and classification

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12 December 2020

Genomic screen and follow-up analysis for autistic disorder.

1 reference

12 December 2020

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

1 reference

12 December 2020

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

1 reference

12 December 2020

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

1 reference

12 December 2020

10.1007/S10038-003-0064-9

Identifiers

DOI

1 reference

release_is4kv4givbh5pjtohsnnex5ole

7 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/is4kv4givbh5pjtohsnnex5ole

24 November 2022

mapped directly with Wikidata item

PubMed ID

13680297

1 reference

PubMed ID

13680297