Hb Showa Yakushiji [β 110 (G12) Leu→Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji-Reference-Cited by-同舟云学术

Hb Showa Yakushiji [β 110 (G12) Leu→Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji

Published:2008-09 Issue:2 Volume:41 Page:166-168
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Colah R.,Nadkarni A.,Gorakshakar A.,Phanasgaonkar S.,Sawant P.,Surve R.,Mohanty D.,Ghosh K.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference9 articles.

1. Application of covalent reverse dot blot hybridization for rapid prenatal diagnosis of common Indian thalassemia syndromes;Colah;Ind. J. of Haemat. & Blood Transfusion,1997

2. Distribution of beta-thalassemia mutations in the Indian population referred to a diagnostic center;Vaz;Hemoglobin,2000

3. Potential of denaturing gradient gel electrophoresis for scanning of β-thalassemia mutations in India;Gorakshakar;Am. J. Hemat.,1999

4. Polymerase chain reaction amplification applied to the determination of β like globin gene cluster haplotypes;Sutton;Am. J. Hematol.,1989

5. Rapid and reliable 7- deletional multiplex polymerase chain reaction assay for alpha thalassemia;Tan;Blood,2001

Cited by 2 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 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