HuGE Literature Finder
Records 1-2
No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.
Orphanet journal of rare diseases 2021 Feb 16 (1): 98. Körber Laura, Schneider Holm, Fleischer Nicole, Maier-Wohlfart Sigr |
PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
Journal of applied oral science : revista FOB 2013 21 (3): 256-64. Wang Jing, Xu Yuanzhi, Chen Jing, Wang Feiyu, Huang Renhuan, Wu Songtao, Shu Linjing, Qiu Jingyi, Yang Zhi, Xue Junjie, Wang Raorao, Zhao Jilin, Lai Wen |
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- Page last updated:Mar 02, 2021
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