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Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis
X-linked congenital generalized hypertrichosis (Online Mendelian Inheritance in Man 307150) is an extremely rare condition of hair overgrowth on different body sites. We previously reported linkage in a large Mexican family with X-linked congenital generalized hypertrichosis cosegregating with deafn...
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主要な著者: | , , , , , , , , , , , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
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National Academy of Sciences
2013
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3651487/ https://ncbi.nlm.nih.gov/pubmed/23603273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1216412110 |
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