Prader–Willi Syndrome: 16-Year Experience in Hong Kong-Reference-Cited by-同舟云学术

Prader–Willi Syndrome: 16-Year Experience in Hong Kong

Published:2012-04 Issue:4 Volume:39 Page:191-194
ISSN:1673-8527
Container-title:Journal of Genetics and Genomics
language:en
Short-container-title:Journal of Genetics and Genomics

Author:

Lo Ivan F.M.,Luk Ho Ming,Tong Tony M.F.,Lai Kent K.S.,Chan Daniel H.C.,Lam Albert C.F.,Chan David K.H.,Hau Edgar W.L.,Fung Connie O.Y.,Lam Stephen T.S.

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology

Reference19 articles.

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2. Prevalence of and risk factors for physical ill health in people with Prader–Willi syndrome: a population based study;Butler;Dev. Med. Child Neurol.,2002

3. Benefits of long-term GH therapy in Prader–Willi syndrome: a 4-year study;Carrel;J. Clin. Endocrinol. Metab.,2002

4. Genetic and behavioural aspects of Prader–Willi syndrome: a review with translation of the original paper;Clarke;Ment. Handicap. Res.,1995

5. A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism;De Smith;Hum. Mol. Genet.,2009

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1. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region;Brain and Behavior;2024-04

2. Effects of early recombinant human growth hormone treatment in young Chinese children with Prader–Willi syndrome;Orphanet Journal of Rare Diseases;2023-02-07

3. Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China;Molecular Cytogenetics;2019-02-18

4. Growth patterns of Chinese patients with Prader-Willi syndrome;Congenital Anomalies;2015-10-26