A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development

BACKGROUND: An ovotesticular disorder of sex development (OT-DSD) was rarely found in human. The mechanism causing such condition is poorly understood. We hereby reported a 11-year-old child with OT-DSD and a karyotype 46,XX/46,XY, a single maternal and double paternal genetic contribution to the pa...

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Detalles Bibliográficos
Autores principales: Xia, Xin-Yi, Wang, Wei-Ping, Li, Tian-Fu, Li, Wei-Wei, Wu, Qiu-Yue, Li, Na, Zhang, Cui, Gao, Hong-Liu, Li, Xiao-Jun, Cui, Ying-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974030/
https://www.ncbi.nlm.nih.gov/pubmed/24581244
http://dx.doi.org/10.1186/1755-8166-7-16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974030/
https://www.ncbi.nlm.nih.gov/pubmed/24581244
http://dx.doi.org/10.1186/1755-8166-7-16

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