The Rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in Combination with an α Gene Triplication Found in a Dutch Patient During Her First Pregnancy Examination-Reference-Cited by-同舟云学术

The Rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in Combination with an α Gene Triplication Found in a Dutch Patient During Her First Pregnancy Examination

Published:2007-01 Issue:2 Volume:31 Page:167-171
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Giordano Piero C.,Addo-Daaku Akosua,Sander Margaretha J.,van Rooijen-Nijdam Irene,van Delft Peter,Harteveld Cornelis L.,Kok Peter J.M.J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260701288922

Reference9 articles.

1. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

2. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

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1. Hemoglobin Showa-Yakushiji: A Common β Thalassemia Mutation Among the Agri Community from Western India;Genetic Testing and Molecular Biomarkers;2012-04

2. Thalassemia-like Phenotype in a Novel Complex Hemoglobinopathy With α, β, δ Globin Chain Abnormalities;Journal of Pediatric Hematology/Oncology;2011-12

3. Hb Den Haag [β45(CD4)Phe→Tyr]. A New Hemoglobin Variant Observed During Early Pregnancy Diagnostics;Hemoglobin;2010-01

4. Frequency of α-Globin Gene Triplications and Their Interaction with β-Thalassemia Mutations;Hemoglobin;2009-01

5. Hb Showa Yakushiji [β 110 (G12) Leu→Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji;Blood Cells, Molecules, and Diseases;2008-09