Complete and partial XY sex reversal associated with terminal deletion of 10q: Report of 2 cases and literature review
- 15 June 1993
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 46 (5), 597-600
- https://doi.org/10.1002/ajmg.1320460527
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- A further case of monosomy 10qterClinical Genetics, 2008
- Androgen Resistance — The Clinical and Molecular SpectrumNew England Journal of Medicine, 1992
- Terminal deletion of chromosome 10q26 due to a paternal translocation {(7;10)(q36;q26)}American Journal of Medical Genetics, 1991
- Report of the comparative committee for human, mouse and other rodentsCytogenetic and Genome Research, 1991
- Genetic evidence equating SRY and the testis-determining factorNature, 1990
- An unbalanced autosomal translocation (7;9) associated with feminizationClinical Genetics, 1988
- Female external genitalia and müllerian duct derivatives in a 46,XY infant with the Smith‐Lemli‐Opitz syndromeAmerican Journal of Medical Genetics, 1987
- GENETIC CONTROL OF PRIMARY SEX DETERMINATION IN MICEAnnual Review of Genetics, 1986
- Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).Journal of Medical Genetics, 1986
- Sex-reversed XY females with campomelic dysplasia are H-Y negativeHuman Genetics, 1981