Unexpected discovery of hemoglobinopathy C/β° thalassemia-Reference-Cited by-同舟云学术

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Unexpected discovery of hemoglobinopathy C/β° thalassemia

Published:2018-09-21 Issue:11 Volume:6 Page:2117-2120
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Bouyarmane Wafaa¹,Uwingabiye Jean¹^ORCID,Biaz Asmaa¹,Rachid Achraf¹,Mechal Youness¹^ORCID,Dami Abdellah¹,Bouhsain Sanae¹,Ouzzif Zhor¹,El Machtani Idrissi Samira¹

Affiliation:

1. Department of Clinical Biochemistry and Toxicology; Mohammed V Military Teaching Hospital; Faculty of Medicine and Pharmacy; Mohammed V University; Rabat Morocco

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ccr3.1815/fullpdf

Reference22 articles.

1. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update;Giardine;Hum Mutat,2007

2. Les hémoglobines normales et pathologiques;Baudin;Revue Francophone des Laboratoires,2016

3. De Montalembert M Syndromes thalassémiques 2002

4. Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity;Agouti;Genet Test,2008

5. Labie D Elion J Bases moléculaires et physiopathologiques des maladies de l'hémoglobine 2005

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