Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease
Authors:
- Candy Sue Márquez-ÁvilaCandy Sue Márquez-Ávila
- Alfredo Vizcaíno-AlarcónAlfredo Vizcaíno-Alarcón
- Constanza García-DelgadoConstanza García-Delgado
- Paulina María Núñez-MartínezPaulina María Núñez-Martínez
- Francisco Flores-RamírezFrancisco Flores-Ramírez
- Alejandra del Pilar Reyes-De la RosaAlejandra del Pilar Reyes-De la Rosa
- Paola Mendelsberg-FishbeinPaola Mendelsberg-Fishbein
- Diana Ibarra-GrajedaDiana Ibarra-Grajeda
- Patricia Medina-BravoPatricia Medina-Bravo
- Norma Balderrábano-SaucedoNorma Balderrábano-Saucedo
- Salvador Esteva-SolsonaSalvador Esteva-Solsona
- Luz del Carmen Márquez-QuirózLuz del Carmen Márquez-Quiróz
- 8 September 2015
- journal article
- research article
- Published by Elsevier in International Journal of Pediatric Otorhinolaryngology
- Vol. 79 (11) , 1886-1891
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Characteristic Face: A Key Indicator for Direct Diagnosis of 22q11.2 Deletions in Chinese Velocardiofacial Syndrome PatientsPLOS ONE, 2013
- Genotype-phenotype correlation in 22q11.2 deletion syndromeBMC Medical Genetics, 2012
- Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSJournal of Medical Genetics, 2012
- Practical Guidelines for Managing Patients with 22q11.2 Deletion SyndromeThe Journal of Pediatrics, 2011
- Constitutional Growth Delay Pattern of Growth in Velo-Cardio-Facial Syndrome: Longitudinal follow up and final height of two casesJournal of Clinical Research in Pediatric Endocrinology, 2011
- Velo‐cardio‐facial syndrome: 30 Years of studyDevelopmental Disabilities Research Reviews, 2008
- Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: A Korean multicenter studyInternational Journal of Cardiology, 2007
- Defining the Clinical Spectrum of Deletion 22q11.2The Journal of Pediatrics, 2005
- Presenting phenotype in 100 children with the 22q11 deletion syndromeEuropean Journal of Pediatrics, 2004
- Thrombocytopenia in patients with chromosome 22q11.2 deletion syndromeThe Journal of Pediatrics, 2003