Literature DB >> 6547776

A cytological map of the human X chromosome--evidence for non-random recombination.

D A Hartley, K E Davies, D Drayna, R L White, R Williamson.   

Abstract

The cytological location of six cloned DNA sequences on the human X chromosome has been determined to a high resolution by direct hybridisation '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.

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Year:  1984        PMID: 6547776      PMCID: PMC318919          DOI: 10.1093/nar/12.13.5277

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  22 in total

1.  Recombination in male and female meiocytes contrasted.

Authors:  H G Callan; P E Perry
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1977-03-21       Impact factor: 6.237

2.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

3.  Distribution of crossing-over in mouse chromosomes.

Authors:  M F Lyon
Journal:  Genet Res       Date:  1976-12       Impact factor: 1.588

4.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

Review 5.  Special sites in generalized recombination.

Authors:  F W Stahl
Journal:  Annu Rev Genet       Date:  1979       Impact factor: 16.830

6.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

7.  Evolution of sickle variant gene.

Authors:  E Solomon; W F Bodmer
Journal:  Lancet       Date:  1979-04-28       Impact factor: 79.321

8.  Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.

Authors:  M E Harper; G F Saunders
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

9.  DNA content and DNA-based centromeric index of the 24 human chromosomes.

Authors:  M L Mendelsohn; B H Mayall; E Bogart; D H Moore; B H Perry
Journal:  Science       Date:  1973-03-16       Impact factor: 47.728

Review 10.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

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  26 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.

Authors:  D Stambolian; R A Lewis; K Buetow; A Bond; R Nussbaum
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

4.  Enzymatic cleavage of a bacterial genome at a 10-base-pair recognition site.

Authors:  M D Weil; M McClelland
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

Review 5.  Molecular genetics of the human X chromosome.

Authors:  K E Davies
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

6.  Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

Authors:  K E Davies; M G Mattei; J F Mattei; H Veenema; S McGlade; K Harper; N Tommerup; K B Nielsen; M Mikkelsen; P Beighton
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Progress towards construction of a total restriction fragment map of a human chromosome.

Authors:  H Vissing; F Grosveld; E Solomon; G Moore; N Lench; N Shennan; R Williamson
Journal:  Nucleic Acids Res       Date:  1987-02-25       Impact factor: 16.971

8.  Linkage analysis of X linked retinitis pigmentosa in the Irish population.

Authors:  G J Farrar; M T Geraghty; J M Moloney; D J McConnell; P Humphries
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

9.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

10.  Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.

Authors:  C Hydén-Granskog; R Salonen; H von Koskull
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

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