Molecular Variations Linked to the Grouping of β- and α-Globin Genes in Neonatal Patients with Sickle Cell Disease in the State of Pernambuco, Brazil-Reference-Cited by-同舟云学术

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Molecular Variations Linked to the Grouping of β- and α-Globin Genes in Neonatal Patients with Sickle Cell Disease in the State of Pernambuco, Brazil

Published:2007-01 Issue:1 Volume:31 Page:83-88
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Bezerra Marcos André C.,Santos Magnun N.N.,Araújo Aderson S.,Gomes Yara M.,Abath Frederico G.C.,Bandeira Flavia M.G.C.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260601057153

Reference20 articles.

1. Characteristics of hemoglobin

2. β-Globin gene haplotype in Hb SC disease

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2. Timed Average Mean Maximum Velocity (TAMMV) of Cerebral Blood Flow of Children and Adolescents with Sickle cell Disease: correlation with clinical and hematological profiles in country;Malawi Medical Journal;2021-09-27

3. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort;Annals of Hematology;2021-02-13

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