Genetic variation affects de novo translocation frequency

Takema Kato, Hidehito Inagaki, Kouji Yamada, Hiroshi Kogo, Tamae Ohye, Hiroe Kowa, Kayuri Nagaoka, Mariko Taniguchi, Beverly S. Emanuel, Hiroki Kurahashi

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

A palindromic sequence on human chromosome 11 causes frequent translocations during meiosis, while a more recently evolved nonpalindromic allele does not.

Original languageEnglish
Number of pages1
JournalScience
Volume311
Issue number5763
DOIs
Publication statusPublished - 17-02-2006

All Science Journal Classification (ASJC) codes

  • General

Fingerprint Dive into the research topics of 'Genetic variation affects de novo translocation frequency'. Together they form a unique fingerprint.

  • Cite this