(Q52113969)

English

A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS.

scientific article published in October 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS. (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

author name string

Webb T

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Whittington J

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Clarke D

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Boer H

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Butler J

5

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Holland A

6

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

publication date

1 October 2002

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Clinical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

62

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

273-281

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Towards a molecular understanding of Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Prader-Willi and Angelman syndromes: sister imprinted disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Obsessions and compulsions in Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

The third factor of the WISC-III: it's (probably) not freedom from distractibility

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Neuropsychological factors associated with borderline pathology in children

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620404.X

21 January 2018

Identifiers

10.1034/J.1399-0004.2002.620404.X

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

release_lwponelt2vbsbc477z7tpndale

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https://api.fatcat.wiki/v0/release/lwponelt2vbsbc477z7tpndale

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/12372053

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