Literature DB >> 6173167

Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2, and 9.

D A Laurie, M Hultén, G H Jones.   

Abstract

Chiasma frequency and the distribution of chiasmata within chromosomes 1, 2, and 9 were investigated in a total of seven males with presumptively normal meiosis. With the exception of one unusual individual there was little variation among the males examined for these characteristics. The exceptional male had a reduced chiasma frequency, which, rather than being considered abnormal, was thought to represent the lower end of the normal range of variability. A statistical analysis of the histograms of chiasma distribution confirmed the impression of overall similarity, and we conclude that genetic maps of these chromosomes may now be constructed without too much disturbance from differences between individuals. The maps will be presented separately in a subsequent paper.

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Year:  1981        PMID: 6173167     DOI: 10.1159/000131641

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  15 in total

1.  Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13).

Authors:  A S Goldman; R H Martin; R Johannisson; C P Gould; E V Davison; J E Emslie; J Burn; M A Hultén
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

2.  Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Authors:  G M Brown; M Leversha; M Hulten; M A Ferguson-Smith; N A Affara; R A Furlong
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

3.  The extent, mechanism, and consequences of genetic variation, for recombination rate.

Authors:  W P Robinson
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

Review 4.  Molecular genetics of the human X chromosome.

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

5.  Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

Authors:  M Patterson; S Kenwrick; S Thibodeau; K Faulk; M G Mattei; J F Mattei; K E Davies
Journal:  Nucleic Acids Res       Date:  1987-03-25       Impact factor: 16.971

6.  Estimating meiotic exchange patterns from recombination data: an application to humans.

Authors:  N E Lamb; E Feingold; S L Sherman
Journal:  Genetics       Date:  1997-07       Impact factor: 4.562

7.  Do chiasmata disappear? An examination of whether closely spaced chiasmata are liable to reduction or loss.

Authors:  C Tease; G H Jones
Journal:  Chromosome Res       Date:  1995-05       Impact factor: 5.239

8.  Genetic mapping: X chromosome.

Authors:  B Keats
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype.

Authors:  D A Laurie; R W Palmer; M A Hultén
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Variation in meiotic recombination frequencies among human males.

Authors:  Fei Sun; Kiril Trpkov; Alfred Rademaker; Evelyn Ko; Renée H Martin
Journal:  Hum Genet       Date:  2004-12-01       Impact factor: 4.132

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