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
Wiktor Borozdin, Ana M. Bravo Ferrer Acosta, Michael J. Bamshad, Elke M. Botzenhart, Ursula G. Froster, Johannes Lemke, Albert Schinzel, Stephanie Spranger, Julie McGaughran, Dorothea Wand, Krystyna HVolume:
27
Année:
2006
Langue:
english
Pages:
2
DOI:
10.1002/humu.9449
Fichier:
PDF, 151 KB
english, 2006