A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome)

Title
A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome)
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 79, Issue 2, Pages 183-188
Publisher
Wiley
Online
2010-04-14
DOI
10.1111/j.1399-0004.2010.01449.x

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