Literature DB >> 3359671

Translocation t(13;14) in nine generations with a case of translocation homozygosity.

A Eklund1, K O Simola, M Ryynänen.   

Abstract

The Robertsonian translocation 5(13;14)(p11;q11) was studied in three families with probable common ancestry in Eastern Finland. In the largest family the translocation has segregated through at least nine generations. The same family also included a female who was homozygous for t(13;14). No clear-cut effect of the translocation on fertility could be demonstrated and only one case of trisomy 13 was recorded in the offspring of t(13;14) carriers. The results are discussed, with implication for human chromosomal evolution.

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Year:  1988        PMID: 3359671     DOI: 10.1111/j.1399-0004.1988.tb03415.x

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


  3 in total

1.  Homozygosity for a Robertsonian Translocation (13q;14q) in a Phenotypically Normal 44, XX Female with a History of Recurrent Abortion and a Normal Pregnancy Outcome.

Authors:  Mohammad Miryounesi; Mehdi Diantpour; Elahe Motevaseli; Soudeh Ghafouri-Fard
Journal:  J Reprod Infertil       Date:  2016 Jul-Sep

2.  One pedigree we all may have come from - did Adam and Eve have the chromosome 2 fusion?

Authors:  Paweł Stankiewicz
Journal:  Mol Cytogenet       Date:  2016-09-26       Impact factor: 2.009

Review 3.  The telomeric sync model of speciation: species-wide telomere erosion triggers cycles of transposon-mediated genomic rearrangements, which underlie the saltatory appearance of nonadaptive characters.

Authors:  Reinhard Stindl
Journal:  Naturwissenschaften       Date:  2014-02-04
  3 in total

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