Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq
- 1 January 1989
- journal article
- Published by Wiley in Annals of Human Genetics
- Vol. 53 (1), 9-14
- https://doi.org/10.1111/j.1469-1809.1989.tb01117.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Deletions of the steroid sulphatase gene in ?classical? X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeHuman Genetics, 1987
- Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.Proceedings of the National Academy of Sciences, 1987
- Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)Nucleic Acids Research, 1987
- Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypesNucleic Acids Research, 1987
- Steroid sulphatase and the conservation of mammalian X chromosomesTrends in Genetics, 1986
- Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X- chromosome and autosomal sequencesNucleic Acids Research, 1986
- Homologous expressed genes in the human sex chromosome pairing regionNature, 1985
- X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked alleleNature, 1985
- A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armNucleic Acids Research, 1984
- Genetic homology and crossing over in the X and Y chromosomes of mammalsHuman Genetics, 1982