(Q50306507)

2 March 2018

title

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study. (English)

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2 March 2018

author name string

Marijcke W M Veltman

1

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2 March 2018

Russell J Thompson

2

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Ellen E Craig

3

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Nicholas R Dennis

4

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Sian E Roberts

5

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Vanessa Moore

6

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Josie A Brown

7

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Patrick F Bolton

8

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language of work or name

English

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publication date

1 February 2005

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2 March 2018

Journal of Autism and Developmental Disorders

published in

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2 March 2018

volume

35

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2 March 2018

issue

1

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2 March 2018

page(s)

117-127

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2 March 2018

https://scigraph.springernature.com/pub.10.1007/s10803-004-1039-1

exact match

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cites work

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12 December 2020

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12 December 2020

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Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

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Annotation: tuberous sclerosis

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12 December 2020

A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus

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12 December 2020

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

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12 December 2020

A case-control family history study of autism

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12 December 2020

Genetic studies of autism: from the 1970s into the millennium

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12 December 2020

Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients

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12 December 2020

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

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12 December 2020

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay

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12 December 2020

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder

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12 December 2020

Autism screening questionnaire: diagnostic validity.

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12 December 2020

A case of autism associated with partial tetrasomy 15

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12 December 2020

10.1007/S10803-004-1039-1

Identifiers

DOI

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2 March 2018

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2 March 2018