Literature DB >> 6449251

[Chromosomal changes in evolution and in pathology: analysis of pericentric inversions].

B Dutrillaux, A Aurias, E Viegas-Péquignot.   

Abstract

The great similarities between pericentric inversions observed in human pathology, having occurred during evolution, or radio-induced in human cells, indicate that they do not occur at random. About 1/3rd to 1/4th of these chromosomal rearrangements are capable to induce abnormal progeny after aneusomy of recombination, during meiosis.

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Year:  1980        PMID： 6449251

Source DB:  PubMed          Journal:  C R Seances Soc Biol Fil        ISSN： 0037-9026


  4 in total

1.  Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States.

Authors:  A C Smith; K Spuhler; T M Williams; T McConnell; E Sujansky; A Robinson
Journal:  Am J Hum Genet       Date:  1987-12       Impact factor: 11.025

Review 2.  The nuclear skeleton and the spatial arrangement of chromosomes in the interphase nucleus of vertebrate somatic cells.

Authors:  J Hubert; C A Bourgeois
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

3.  A Rare Case of Pericentric Inversion, Inv (21) (p12;q22) in Repeated Pregnancy Loss: A Case Report.

Authors:  Naeimeh Tayebi; Hossain Khodaei
Journal:  Oman Med J       Date:  2011-11

4.  Direct evidence for suppression of recombination within two pericentric inversions in humans: a new sperm-FISH technique.

Authors:  M Jaarola; R H Martin; T Ashley
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025
  4 in total

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