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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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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
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| Assuntos: | |
| Acesso em linha: | 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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