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Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates

✍ Scribed by Christine J. Shaw; Marjorie A. Withers; James R. Lupski


Book ID
117854462
Publisher
American Society of Human Genetics
Year
2004
Tongue
English
Weight
672 KB
Volume
75
Category
Article
ISSN
0002-9297

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