Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
- 30 April 1990
- Vol. 61 (4) , 603-610
- https://doi.org/10.1016/0092-8674(90)90472-q
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- A long range restriction map of the distal human X chromosome short arm around the steroid sulfatase locusNucleic Acids Research, 1990
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosomeNucleic Acids Research, 1989
- Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levelsGenomics, 1989
- A rapid procedure for colony screening using nylon filtersNucleic Acids Research, 1989
- X Chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis)Human Genetics, 1988
- Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesGenomics, 1988
- Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)Nucleic Acids Research, 1987
- Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfataseBiochemical and Biophysical Research Communications, 1987
- Hypervariable ‘minisatellite’ regions in human DNANature, 1985