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Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11
Roy Wadey, Judith McKie, Charalambos Papapetrou, Helen Sutherland, Frans Lohman, Jan Osinga, Ingrid Frohn, Robert Hofstra, Carel Meijers, Francesca Amati, Emanuela Conti, Antonio Pizzuti, Bruno DallapVolume:
65
Year:
1999
Language:
english
DOI:
10.1086/302468
File:
PDF, 52 KB
english, 1999