Malcolm Russell Whitman, Ph.D.
This page shows the publications Malcolm Whitman has written about Female.
A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome. Am J Med Genet A. 2013 Aug; 161A(8):2040-6.
New roles for FoxH1 in patterning the early embryo. Development. 2004 Oct; 131(20):5065-78.
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