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Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14)
Turner syndrome is a common sex chromosome disorder characterized by complete or partial absence of an X chromosome. The spectrum of its clinical features and cytogenetics are various. We report new chromosomal formula revealed by DSD and associated with translocation (13,14). To our knowledge, this...
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| Publicat a: | Case Rep Endocrinol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6311845/ https://ncbi.nlm.nih.gov/pubmed/30647978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/3796415 |
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