Zobrazeno 1 - 1
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pro vyhledávání: '"OrighoyeTosan Temisanren"'
Autor:
BabatundeOludare Fakuade, Ahmed Iya Girei, FadekemiAdetutu Ajibade, OrighoyeTosan Temisanren, Saleh Yuguda
Publikováno v:
Sahel Medical Journal, Vol 22, Iss 4, Pp 200-206 (2019)
Background: Sickle cell anemia is a hereditary disorder of the hematological system. It involves the production of abnormal hemoglobin, which is sickle in shape and has a short life span, resulting in secondary hemopoietic function by the long bones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd02b154893a18a29e5320b350f95d8
http://www.smjonline.org/article.asp?issn=1118-8561
http://www.smjonline.org/article.asp?issn=1118-8561
