Hemoglobin SO-Arab and α-Thalassemia Diagnosed in an Adult: A Case-based Review of the Hemoglobinopathies-Reference-Cited by-同舟云学术

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Hemoglobin SO-Arab and α-Thalassemia Diagnosed in an Adult: A Case-based Review of the Hemoglobinopathies

Published:2013-10 Issue:4 Volume:346 Page:325-327
ISSN:0002-9629
Container-title:The American Journal of the Medical Sciences
language:en
Short-container-title:The American Journal of the Medical Sciences

Author:

Zacharia George,Maronge Genevieve F.,Boulmay Brian C.,Brazda Frederick W.,Lopez Fred A.

Publisher

Elsevier BV

Subject

General Medicine

Reference24 articles.

1. Global epidemiology of haemoglobin disorders and derived service indicators;Modell;Bull World Health Organ,2008

2. Evidence for both innate and acquired mechanisms of protection from Plasmodium falciparum in children with sickle cell trait;Gong;Blood,2012

3. The population genetics and dynamics of the thalassemias;Weatherall;Hematol Oncol Clin North Am,2010

4. Laboratory investigation of hemoglobinopathies and thalassemias: review and update;Clarke;Clin Chem,2000

5. Population estimates of sickle cell disease in the U;Hassell;S. Am J Prev Med,2010

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemoglobin S/OArab: Retinal Manifestations of a Rare Hemoglobinopathy;Case Reports in Ophthalmology;2020-05-27

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