Literature DB >> 4073834

Further studies on chiasma distribution and interference in the human male.

D A Laurie, M A Hultén.   

Abstract

Some unusual patterns of chiasma distribution were noted in a preliminary investigation of meiosis in an infertile male with an apparently normal mitotic karyotype and a normal mean autosomal cell chiasma frequency. A detailed investigation of chiasma distribution on all 22 autosomes revealed that several chromosomes showed a significant change in chiasma distribution and/or mean inter-chiasma distance in comparison with previously published controls. These findings are discussed in relation to the general patterns of chiasma localization in the human male and the role of interference.

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Year:  1985        PMID： 4073834     DOI： 10.1111/j.1469-1809.1985.tb01694.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


  37 in total

1.  Characterization of human crossover interference.

Authors:  K W Broman; J L Weber
Journal:  Am J Hum Genet       Date:  2000-05-08       Impact factor: 11.025

2.  Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

Authors:  Sue Ann Berend; Scott L Page; William Atkinson; Christopher McCaskill; Neil E Lamb; Stephanie L Sherman; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-12-23       Impact factor: 11.025

Review 3.  Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis.

Authors:  Frédéric Baudat; Bernard de Massy
Journal:  Chromosome Res       Date:  2007       Impact factor: 5.239

4.  Sex-chromosome pairing: evidence that the behavior of the pseudoautosomal region differs during male and female meiosis.

Authors:  P A Hunt; R LeMaire
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

Review 5.  Chromosome bands, their chromatin flavors, and their functional features.

Authors:  G P Holmquist
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

6.  A recombination map of the human X-chromosome.

Authors:  R G Del Mastro; P A Farndon; M W Kilpatrick
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

7.  The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

Authors:  P Simi; M Ceccarelli; A Barachini; G Floridia; O Zuffardi
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

8.  Two-parameter characterization of chromosome-scale recombination rate.

Authors:  Wentian Li; Jan Freudenberg
Journal:  Genome Res       Date:  2009-09-14       Impact factor: 9.043

9.  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

10.  Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval.

Authors:  F Rodius; F Duclos; K Wrogemann; D Le Paslier; P Ougen; A Billault; S Belal; C Musenger; A Brice; A Dürr
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025
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