Report of Fertility in a Woman with a Predominantly 46,XY Karyotype in a Family with Multiple Disorders of Sexual Development

Context: We report herein a remarkable family in which the mother of a woman with 46,XY complete gonadal dysgenesis was found to have a 46,XY karyotype in peripheral lymphocytes, mosaicism in cultured skin fibroblasts (80% 46,XY and 20% 45,X) and a predominantly 46,XY karyotype in the ovary (93% 46,...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Dumic, Miroslav, Lin-Su, Karen, Leibel, Natasha I., Ciglar, Srecko, Vinci, Giovanna, Lasan, Ruzica, Nimkarn, Saroj, Wilson, Jean D., McElreavey, Ken, New, Maria I.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: The Endocrine Society 2008
Θέματα:
Original Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2190741/
https://ncbi.nlm.nih.gov/pubmed/18000096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2007-2155
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