Expanding the spectrum of TBX5 mutations in Holt‐Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations
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M. Bamshad | K. Chrzanowska | J. Mcgaughran | J. Lemke | J. Kohlhase | D. Wand | E. Botzenhart | U. Froster | S. Spranger | W. Borozdin | A. Schinzel | Ana M. Bravo Ferrer Acosta | J. McGaughran