High rates of de novo 15q11q13 inversions in human spermatozoa
<p>Abstract</p> <p>Low-Copy Repeats predispose the 15q11-q13 region to non-allelic homologous recombination. We have already demonstrated that a significant percentage of Prader-Willi syndrome (PWS) fathers have an increased susceptibility to generate 15q11q13 deletions in spermato...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-02-01
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Series: | Molecular Cytogenetics |
Subjects: | |
Online Access: | http://www.molecularcytogenetics.org/content/5/1/11 |