| Literature DB >> 19361780 |
Anna Biason-Lauber1, Daniel Konrad, Monika Meyer, Carine DeBeaufort, Eugen J Schoenle.
Abstract
A girl with a prenatal 46,XY karyotype was born with a completely normal female phenotype, including uterus and histologically normal ovaries. In mice with a similar phenotype, the ablation of M33, an ortholog of Drosophila Polycomb, causes male-to-female sex reversal. The analysis of the human homolog of M33, Chromobox homolog 2 (CBX2), in this girl revealed loss-of-function mutations that allowed us, by placing CBX2 upstream of SRY, to add an additional component to the still incomplete cascade of human sex development.Entities:
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Year: 2009 PMID: 19361780 PMCID: PMC2680992 DOI: 10.1016/j.ajhg.2009.03.016
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025