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Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency

Detalles Bibliográficos
Autores principales:	Ji, Wen, Zhang, Lu-Yao, Li, Fu-Cheng, Wang, Yu, He, Wei, Yin, Qi-Qi, Liao, Zhi-Hong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427800/ https://www.ncbi.nlm.nih.gov/pubmed/26780871 http://dx.doi.org/10.4103/1008-682X.170865

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