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Failure to recombine is a common feature of human oogenesis

  • Published:2021-01 Issue:1 Volume:108 Page:16-24
  • ISSN:0002-9297
  • Container-title:The American Journal of Human Genetics
  • language:en
  • Short-container-title:The American Journal of Human Genetics

Author:

Hassold Terry,Maylor-Hagen Heather,Wood Anna,Gruhn Jennifer,Hoffmann Eva,Broman Karl W.,Hunt Patricia

Funder

Novo Nordisk

National Institutes of Health

Danmarks Grundforskningsfond

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Human aneuploidy: mechanisms and new insights into an age-old problem;Nagaoka;Nat. Rev. Genet.,2012

2. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16;Hassold;Am. J. Hum. Genet.,1995

3. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II;Lamb;Nat. Genet.,1996

4. Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors;Thomas;Hum. Mol. Genet.,2001

5. Non-disjunction of chromosome 13;Bugge;Hum. Mol. Genet.,2007

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