Mutation Analysis of Fibrillin-2 (FBN2) and Microfibril Associated Protein-3 (MFAP-3): Two Genes Associated With Congenital Contractural Arachnodactyly (CCA), Also Known as Beal's Syndrome
doi 10.15760/etd.7073
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Date
January 1, 2000
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Portland State University Library