Unequal Meiotic Crossover: A Frequent Cause of NF1 Microdeletions
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
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3. Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome;Carrozzo;Am J Hum Genet,1997
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