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Novel FGFR1 and KISS1R Mutations in Chinese Kallmann Syndrome Males with Cleft Lip/Palate

Kallmann syndrome (KS) is characterized by isolated hypogonadotropic hypogonadism (IHH) with anosmia and is sometimes associated with cleft lip/palate (CLP). In order to describe the clinical features, genetic etiology, and treatment outcome of KS males with CLP, we performed genetic screening for 1...

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Bibliografiset tiedot
Julkaisussa:Biomed Res Int
Päätekijät: Xu, Hao, Niu, Yonghua, Wang, Tao, Liu, Simin, Xu, Hua, Wang, Shaogang, Liu, Jihong, Ye, Zhangqun
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4496468/
https://ncbi.nlm.nih.gov/pubmed/26199944
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/649698
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