Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 3 (of 3 Records)

Query Trace: Prader-Willi Syndrome and NDN[original query]
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2001 Jun 25 (6): 767-9.
Oeffner F, Korn T, Roth H, Ziegler A, Hinney A, Goldschmidt H, Siegfried W, Hebebrand J, Grzeschik K
Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.
Obesity (Silver Spring, Md.) 2011 Jun 19 (6): 1229-34.
Chen Yuan, Liu Yong-Jun, Pei Yu-Fang, Yang Tie-Lin, Deng Fei-Yan, Liu Xiao-Gang, Li Ding-You, Deng Hong-W
Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.
The Journal of clinical endocrinology and metabolism 2020 6 105 (8): 2732-9.
Meader Brooke N, Albano Alessandro, Sekizkardes Hilal, Delaney Ange
TOP