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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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| Publicado no: | Case Rep Endocrinol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2018
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| Assuntos: | |
| Acesso em linha: | 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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