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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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3974030/
https://ncbi.nlm.nih.gov/pubmed/24581244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-7-16
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