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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Bibliografski detalji

Glavni autori:	Paula Sandrin-Garcia, Antonio Richieri-Costa, Eloiza Helena Tajara, Andréa Borduchi Carvalho-Salles, Agnes Cristina Fett-Conte
Format:	Artigo
Jezik:	Inglês
Izdano:	Sociedade Brasileira de Genética 2007-01-01
Serija:	Genetics and Molecular Biology
Teme:	velocardiofacial syndrome 22q11.2 deletion
Online pristup:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572007000100006
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