Transcription Factor Pathways and Congenital Heart Disease

Author:

McCulley David J.,Black Brian L.

Publisher

Elsevier

Reference208 articles.

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2. Associated anomalies in asymmetric crying facies and 22q11 deletion;Akcakus;Genet. Couns.,2003

3. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations;Alikasifoglu;Turk. J. Pediatr.,2000

4. Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease;Baekvad-Hansen;Am. J. Med. Genet. A,2006

5. Mowat-Wilson syndrome: The first two Malaysian cases;Balasubramaniam;Singapore Med. J.,2010

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