The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient-Reference-Cited by-同舟云学术

The Ivs-1-110 (G→T) and Codon 39 (C→T) β-Thalassemia Mutations in Association with α-Thal-2 (−3.7 Kb) and Hb Hasharon [α47(CE5)Asp→His] in a Brazilian Patient

Published:1992-01 Issue:6 Volume:16 Page:525-528
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Costa F. F.,Figueredo M. S.,Sonati M. F.,Kimura E. M.,Martins C. S. B.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269208993122

Reference8 articles.

1. Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia

2. Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes

3. Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.

4. Hemoglobin Stanleyville II (?78 Asn?Lys) is associated with a 3.7-kb ?-globin gene deletion

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3. “N-rasGene Point Mutations in Brazilian Acute Myelogenous Leukemia Patients Correlate with a Poor Prognosiss”;Leukemia & Lymphoma;1997-01

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