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Role of hypocalcemia in identification of 22q11 deletion syndrome among patients with congenital heart defects
Authors:Vinicius Freitas de Mattos,Leonardo Paludo Sulczinski,Olga Gaio Milner,Filipe Augusto da Silva,Samir Abou Ghaouche de Moraes,Patrí  cia Trevisan,Marilu Fiegenbaum,Marileila Varella-Garcia,Paulo Ricardo Gazzola Zen,Rafael Fabiano Machado Rosa
Affiliation:1. Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil;2. Graduation in Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil;3. Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil;4. Human Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil;5. School of Medicine, Division of Medical Oncology, University of Colorado Denver, CO, USA;6. Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil
Abstract:
Keywords:Calcium   Velocardiofacial syndrome   Cardiac malformations   FISH   Screening
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