Wird geladen...

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomed Res Int
Hauptverfasser: Xu, Hao, Niu, Yonghua, Wang, Tao, Liu, Simin, Xu, Hua, Wang, Shaogang, Liu, Jihong, Ye, Zhangqun
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi Publishing Corporation 2015
Schlagworte:
Online Zugang: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
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!