Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies

Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies

The velocardiofacial syndrome (VCFS), a condition associated with 22q11.2 deletions, is characterized by a typical facies, palatal anomalies, learning disabilities, behavioral disturbances and cardiac defects. We investigated the frequency of these chromosomal deletions in 16 individuals with VCFS f...

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Bibliographic Details
Main Authors:	Paula Sandrin-Garcia, Antonio Richieri-Costa, Eloiza Helena Tajara, Andréa Borduchi Carvalho-Salles, Agnes Cristina Fett-Conte
Format:	Article
Language:	English
Published:	Sociedade Brasileira de Genética 2007-01-01
Series:	Genetics and Molecular Biology
Subjects:	velocardiofacial syndrome 22q11.2 deletion
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572007000100006

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