Literature DB >> 752505

The use and limitations of chiasma scoring with reference to human genetic mapping.

M Hultén, J M Luciani, V Kirton, M Devictor-Vuillet.   

Abstract

Human chiasma data are summarized, and some preliminary new observations in fetal oocytes are presented. Male chiasma data may give reliable estimates of genetic lengths, both for individual chromosome arms and for the total autosomal complement. Female data are as yet less accurate and give information according to chromosome group only. Movement of chiasmata before they can be reliably scored is unlikely. In both sexes, chiasmata are seen to be clustered along the length of the chromosomes, which may reflect crossingover interference and a tendency for crossingover to more often take place in certain chromosome segments; there are some indications of sex differences in these preferences.

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Year:  1978        PMID: 752505     DOI: 10.1159/000130917

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


  7 in total

1.  Status of the search for a major genetic locus for affective disorder in the Old Order Amish.

Authors:  A J Pakstis; J R Kidd; C M Castiglione; K K Kidd
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

2.  Integration of gene maps: chromosome 21.

Authors:  S Lawrence; A Collins; B J Keats; M Hulten; N E Morton
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

Review 3.  Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors:  H Moser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus.

Authors:  R W Palmer; M A Hultén
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

5.  A pachytene map of the mouse oocyte.

Authors:  G Jagiello; J S Fang
Journal:  Chromosoma       Date:  1980       Impact factor: 4.316

6.  Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism.

Authors:  P Wieacker; N Horn; P Pearson; T F Wienker; E McKay; H H Ropers
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Genetically determined asynapsis, spermatogenic degeneration, and infertility in men.

Authors:  R S Chaganti; S C Jhanwar; L T Ehrenbard; I A Kourides; J J Williams
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

  7 in total

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