A de novo frameshift mutation of the SRY gene leading to a patient with 46,XY complete gonadal dysgenesis

Detalles Bibliográficos
Autores principales: Wang, Xiao-Bo, Liang, Yu-Long, Zhu, Zi-Jue, Zhu, Yong, Li, Peng, Cao, Jia-Ping, Zhang, Qun-Ying, Liu, Qiang, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732898/
https://www.ncbi.nlm.nih.gov/pubmed/30785124
http://dx.doi.org/10.4103/aja.aja_123_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732898/
https://www.ncbi.nlm.nih.gov/pubmed/30785124
http://dx.doi.org/10.4103/aja.aja_123_18

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