Turner syndrome caused by rare complex structural abnormalities involving chromosome X

Turner syndrome (TS) is a phenotypic heterogeneous genetic disorder caused by the loss of an X-chromosome or X-structural abnormalities in the X-chromosome, and affects approximately 1 in every 2,500 females. The affected individuals may develop diverse clinical features, including short stature, ov...

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Bibliographic Details
Published in:Exp Ther Med
Main Authors: Li, Niu, Zhao, Li, Li, Juan, Ding, Yu, Shen, Yongnian, Huang, Xiaodong, Wang, Xiumin, Wang, Jian
Format: Artigo
Language:Inglês
Published: D.A. Spandidos 2017
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5609171/
https://ncbi.nlm.nih.gov/pubmed/28962153
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2017.4756
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