Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and NDN[original query] |
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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 |
Is prone sleeping dangerous for neonates? Polysomnographic characteristics and NDN gene analysis. Ci ji yi xue za zhi = Tzu-chi medical journal 0 31 (2): 113-117. Wong Shi-Bing, Zhao Lu-Lu, Chuang Shu-Hua, Tsai Wen-Hsin, Yu Chun-Hsien, Tsai Li-Pi |
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 |
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