Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System-Reference-Cited by-同舟云学术

Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System

Published:2012-01-12 Issue:2 Volume:36 Page:196-199
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Tang Hai-Shen,Zhou Jian-Ying,Xie Xing-Mei,Li Ru,Liao Can,Li Dong-Zhi

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2011.649151

Reference9 articles.

1. Screening for Hb Constant Spring in the Guangdong Province, South China, Using the Sebia Capillary Electrophoresis System

2. Globin structural mutant α125Leu→Pro is a novel cause of α-thalassaemia

3. Detection of the HB Quong SZE Mutation in a Chinese Family by Selective Amplification of the α2-Globin Gene and Restriction Map Analysis with MSP I

4. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients

5. Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system

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1. Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China;Hemoglobin;2020-03-03

2. Capillary Electrophoresis Based on the Nucleic Acid Detection in the Application of Human Disease Diagnosis;Clinical Laboratory;2014

3. Prenatal control of nondeletional α -thalassemia: first experience in mainland China;Prenatal Diagnosis;2013-05-21

4. CODON 62 (G TG > G CG, Val -> Ala) (alpha 1) (HBA1: c.188T > C) CAUSING NONDELETIONAL alpha-THALASSEMIA IN A CHINESE FAMILY;HEMOGLOBIN;2013

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