A cytological map of the human X chromosome - evidence for non-random recombination
Open Access
- 1 January 1984
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 12 (13), 5277-5285
- https://doi.org/10.1093/nar/12.13.5277
Abstract
The cytological location of six cloned DNA sequences on the human X chromosome has been determined to a high resolution by direct hybridisa tion ‘in situ’ to metaphase chromosomes. Each locus has been identified using clones which also detect restriction fragment length polymorphisms by Southern hybridisation. The six loci identified are spaced along the chromosome from Xp22 to Xq28. By combining data obtained using this powerful sequence localisation technique with that from hybrid cell panels and from family studies, it is possible to compare physical and genetic distances, and to demonstrate that the frequency of reciprocal genetic exchange is not uniform along the chromosome length.Keywords
This publication has 20 references indexed in Scilit:
- Localization of single copy DNA sequences on G-banded human chromosomes by in situ hybridizationChromosoma, 1981
- CONSTRUCTION OF A GENETIC-LINKAGE MAP IN MAN USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS1980
- SPECIAL SITES IN GENERALIZED RECOMBINATIONAnnual Review of Genetics, 1979
- EVOLUTION OF SICKLE VARIANT GENEThe Lancet, 1979
- Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase IJournal of Molecular Biology, 1977
- Recombination in male and female meiocytes contrastedPhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1977
- Distribution of crossing-over in mouse chromosomesGenetics Research, 1976
- Constitutional chromosomal breakageHuman Genetics, 1976
- DNA Content and DNA-Based Centromeric Index of the 24 Human ChromosomesScience, 1973
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960