Literature DB >> 527245

Chromosome variants and abnormalities detected in 51 married couples with repeated spontaneous abortions.

P Genest.   

Abstract

Chromosome analysis of 51 married couples with repeated spontaneous abortions revealed a normal female karyotype in all wives, whereas 39 (76.5%) husbands showed a normal Y chromosome, 10 (19.6%) a Yq+, one (1.9%) a Yqs and one (1.9%) two Y chromosomes. The high incidence of Yq+ found in this investigation correlates with previous reports and indicates that the risk of spontaneous abortions is increased when the male partner has a large Y chromosome.

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Year:  1979        PMID： 527245     DOI： 10.1111/j.1399-0004.1979.tb01346.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  6 in total

1.  Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers?

Authors:  A Lippman-Hand; M Vekemans
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

2.  The effect of chromosomal polymorphisms on the outcomes of fresh IVF/ICSI-ET cycles in a Chinese population.

Authors:  Xiaojuan Xu; Rui Zhang; Wei Wang; Hongfang Liu; Lin Liu; Bin Mao; Xiangwu Zeng; Xuehong Zhang
Journal:  J Assist Reprod Genet       Date:  2016-08-20       Impact factor: 3.412

3.  Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history.

Authors:  S Schwartz; C G Palmer
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.

Authors:  B D Blumberg; J D Shulkin; J I Rotter; T Mohandas; M M Kaback
Journal:  Am J Hum Genet       Date:  1982-11       Impact factor: 11.025

5.  Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages.

Authors:  Wiem Ayed; Islem Messaoudi; Zouhour Belghith; Wajih Hammami; Imen Chemkhi; Nabila Abidli; Helmy Guermani; Rim Obay; Ahlem Amouri
Journal:  Pan Afr Med J       Date:  2017-09-29

6.  A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis.

Authors:  Heng Gu; Jian-hui Jiang; Jian-ying Li; Ya-nan Zhang; Xing-sheng Dong; Yang-yu Huang; Xin-ming Son; Xinyan Lu; Zheng Chen
Journal:  PLoS One       Date:  2013-10-15       Impact factor: 3.240
  6 in total

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