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Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2
Paula Sandrin-Garcia, Dagma V. M. Abramides, Lúcia R. Martelli, Ester S. Ramos, Antônio Richieri-Costa, Geraldo A. S. PassosVolume:
303
Language:
english
Pages:
9
DOI:
10.1007/s11010-007-9450-5
Date:
September, 2007
File:
PDF, 221 KB
english, 2007