Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Diana S, Rendón C"'
Autor:
María Angélica Wietstruck P, Lina M. González R., Francisco Barriga C, Nicolás Rojas R., Cindy Martínez G., Diana S. Rendón C., Pamela Zúñiga C
Publikováno v:
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Revista chilena de pediatría v.89 n.4 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
Universidad del Rosario
instacron:Universidad del Rosario
Revista chilena de pediatría v.89 n.4 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
Sickle cell disease (SCD) is an autosomal recessive genetic disorder. It is the most frequent structural hemoglobinopathy worldwide, and it is produced by an alteration in the globin chain genes. In Chile, there is no data on the prevalence of SCD si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c951b1e1613f946cf91a489e5e2f906
https://repository.urosario.edu.co/handle/10336/22967
https://repository.urosario.edu.co/handle/10336/22967
Autor:
Pamela, Zúñiga C, Cindy, Martínez G, Lina M, González R, Diana S, Rendón C, Nicolás, Rojas R, Francisco, Barriga C, María Angélica, Wietstruck P
Publikováno v:
Revista chilena de pediatria. 89(4)
Sickle cell disease (SCD) is an autosomal recessive genetic disorder. It is the most frequent structural hemoglobinopathy worldwide, and it is produced by an alteration in the globin chain genes. In Chile, there is no data on the prevalence of SCD si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f0d59e13631de6fe28ea16e3672251a5
https://pubmed.ncbi.nlm.nih.gov/30571829
https://pubmed.ncbi.nlm.nih.gov/30571829
