(Q34325671)

1 August 2017

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

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1 August 2017

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Baker P

1

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1 August 2017

Piven J

series ordinal

2

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1 August 2017

Schwartz S

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3

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1 August 2017

Patil S

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

1 August 1994

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Journal of Autism and Developmental Disorders

1 August 2017

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1 August 2017

24

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1 August 2017

529-535

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1 August 2017

4

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https://scigraph.springernature.com/pub.10.1007/bf02172133

1 August 2017

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cites work

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

12 December 2020

Autism associated with marker chromosome.

1 reference

12 December 2020

Cytogenetic and clinical studies in five cases of inv dup(15)

1 reference

12 December 2020

Etiology of autism: genetic influences

1 reference

12 December 2020

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview.

1 reference

12 December 2020

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

1 reference

12 December 2020

Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues

1 reference

12 December 2020

Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15

1 reference

12 December 2020

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

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12 December 2020

Identifiers

DOI

10.1007/BF02172133

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Dimensions Publication ID

1 August 2017

1040431961

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Fatcat ID

release_e44tcesagjealmfqf767qn6u4u

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Fatcat

https://api.fatcat.wiki/v0/release/e44tcesagjealmfqf767qn6u4u

24 November 2022

mapped directly with Wikidata item

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