| Literature DB >> 1577463 |
B Van der Auwera1, N Van Roy, A De Paepe, J R Hawkins, I Liebaers, S Castedo, J Dumon, F Speleman.
Abstract
XX maleness is the most common condition in which testes develop in the absence of a cytogenetically detectable Y chromosome. Using molecular techniques, it is possible to detect Yp sequences in the majority of XX males. In this study, we could detect Y-specific sequences, including the sex-determining region of the Y chromosome (SRY), using fluorescence in situ hybridization. In 5 out of 6 previously unpublished XX males, SRY was translocated onto the terminal part of an X chromosome. This is the first report in which translocation of an SRY-bearing fragment to an X chromosome in XX males could be directly demonstrated.Entities:
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Year: 1992 PMID: 1577463 DOI: 10.1007/bf00207036
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132