Publication: Disruption of HDX Gene in Premature Ovarian Failure
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Abstract
We present a case of a 19-year-old phenotypically normal girl with premature ovarian failure. Cytogenetic analysis using G banding and fluorescence in situ hybridization (FISH) from cultured peripheral blood lymphocytes of the patient and the family revealed a de novo X;15 translocation and the imbalance to be 46,X,t(X;15)(Xpter → Xq21
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Citation
WoS Q
Q2
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Q2
Source
Systems Biology in Reproductive Medicine
Volume
59
Issue
4
Start Page
218
End Page
222