Twenty Years of Neonatal Screening for Sickle Cell Disease in Brazil: The Challenges of a Continental Country with High Genetic Heterogeneity
Author:
Affiliation:
1. Serviço de Referência em Triagem Neonatal, Brasil
2. Universidade Estadual Paulista, Brasil
3. Universidade Federal do Rio Grande do Sul, Brasil; Hospital Materno Infantil Presidente Vargas, Brasil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics(clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
http://www.scielo.br/pdf/jiems/v9/2326-4594-jiems-9-e20210002.pdf
Reference50 articles.
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2. Advances in sickle cell therapies in the hydroxyurea era;Field JJ;Mol Med,2014
3. Perspective: we need a global solution;Odame I;Nature,2014
4. Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference;Lobitz S;Br J Haematol,2018
5. Historical genetics: spatio temporal analysis of the formation of the Brazilian population;Callegari-Jacques SM;Am J Hum Biol,2003
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