Role of hypocalcemia in identification of 22q11 deletion syndrome among patients with congenital heart defects.

Int J Cardiol

Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil; Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil. Electronic address:

Published: November 2014

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http://dx.doi.org/10.1016/j.ijcard.2014.09.133DOI Listing

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