RAI1 point mutations, CAG repeat variation, and SNP...

RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith–Magenis syndrome

Weimin Bi, G. Mustafa Saifi, Santhosh Girirajan, Xin Shi, Barbara Szomju, Helen Firth, R. Ellen Magenis, Lorraine Potocki, Sarah H. Elsea, James R. Lupski
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Volume:
140A
Year:
2006
Language:
english
Pages:
10
DOI:
10.1002/ajmg.a.31510
File:
PDF, 275 KB
english, 2006
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