Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes-Reference-Cited by-同舟云学术

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Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes

Published:2011-11-02 Issue:3 Volume:20 Page:283-290
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Kim Soo-Jeong,Miller Jennifer L,Kuipers Paul J,German Jennifer Ruth,Beaudet Arthur L,Sahoo Trilochan,Driscoll Daniel J

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2011187.pdf

Reference35 articles.

1. Cassidy SB, Driscoll DJ : Prader-Willi syndrome. Eur J Hum Genet 2009; 17: 3–13.

2. Dykens EM, Cassidy SB, King BH : Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy. Am J Ment Retard 1999; 104: 67–77.

3. Horsthemke B, Buiting K : Genomic imprinting and imprinting defects in humans. Adv Genet 2008; 61: 225–246.

4. Nicholls RD, Knepper JL : Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet 2001; 2: 153–175.

5. Christian SL, Bhatt NK, Martin SA et al: Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb. Genome Res 1998; 8: 146–157.

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