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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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Case Rep Endocrinol
Prif Awduron: Latrech, Hanane, Madar, Houssein, Gaouzi, Ahmed
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Hindawi 2018
Pynciau:
Mynediad Ar-lein: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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