Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region
- 1 October 1990
- Vol. 8 (2) , 263-270
- https://doi.org/10.1016/0888-7543(90)90281-x
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Molecular analysis of deletions in the human β-globin gene cluster: Deletion junctions and locations of breakpointsGenomics, 1990
- A review of the molecular genetics of the human alpha-globin gene clusterBlood, 1989
- Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levelsGenomics, 1989
- Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and YqAnnals of Human Genetics, 1989
- Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosomeHuman Genetics, 1988
- Isolation and characterization of a family of sequences dispersed on the human X chromosomeGenomics, 1988
- 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
- Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomalNature, 1985
- Repeated Sequences in DNAScience, 1968