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The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review

Background: Very few reports are available on human XX ovotesticular disorder of sex development involving SOX3 gene duplication. Here we aim to present a rare case of SOX3 gene duplication in a person from the Chinese population who exhibits XX ovotesticular disorder of sex development. Case Presen...

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Detalles Bibliográficos
Autores principales:	Zhuang, Jianlong, Chen, Chunnuan, Li, Jia, Jiang, Yuying, Wang, Junyu, Wang, Yuanbai, Zeng, Shuhong, Lin, Yiming, Xie, Yingjun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225946/ https://www.ncbi.nlm.nih.gov/pubmed/34178900 http://dx.doi.org/10.3389/fped.2021.682846

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