Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: Report and a review of literature-Reference-Cited by-同舟云学术

Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: Report and a review of literature

Published:2013-04-30 Issue:6 Volume:161 Page:1309-1318
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Liu Anthony P.Y.¹,Tang Wing Fai²,Lau Elizabeth T.,Chan Kelvin Y.K.,Kan Anita S.Y.,Wong Kar Yin¹,Tso Winnie W.Y.¹,Jalal Khair¹,Lee So Lun¹,Chau Christy S.K.¹,Chung Brian H.Y.

Affiliation:

1. Department of Paediatrics and Adolescent Medicine; Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong; Hong Kong Special Administrative Region; China

2. Department of Obstetrics and Gynaecology, Li Ka Shing Faculty of Medicine; The University of Hong Kong; Hong Kong Special Administrative Region; China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35909/fullpdf

Reference33 articles.

1. Prader-Willi syndrome and Angelman syndrome;Buiting;Am J Med Genet Part C,2010

2. Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome;Butler;Am J Med Genet Part A,2008

3. An interstitial 15q11-q14 deletion: Expanded Prader-Willi syndrome phenotype;Butler;Am J Med Genet Part A,2010

4. Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q;Calounova;Am J Med Genet Part A,2008

5. Pulmonary interstitial glycogenosis: A new variant of neonatal interstitial lung disease;Canakis;Am J Respir Crit Care Med,2002

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