Newborn screening for α-thalassaemia by a capillary electrophoresis method-Reference-Cited by-同舟云学术

Newborn screening for α-thalassaemia by a capillary electrophoresis method

Published:2012-09 Issue:3 Volume:19 Page:159-159
ISSN:0969-1413
Container-title:Journal of Medical Screening
language:en
Short-container-title:J Med Screen

Author:

Tang Hai-Shen¹,Zhou Jian-Ying¹,Xie Xing-Mei¹,Li Dong-Zhi¹

Affiliation:

1. Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Women & Children Medical Center, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health Policy

Link

http://journals.sagepub.com/doi/pdf/10.1258/jms.2012.012100

Reference6 articles.

1. Relationship between neonatal screening results by HPLC and the number of α-thalassaemia gene mutations; consequences for the cut-off value

2. Heterogeneity of Hemoglobin H Disease in Childhood

3. Newborn Screening for α-Thalassemia — Keeping Up with Globalization

4. Weighing the Evidence for Newborn Screening for Hemoglobin H Disease

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

Cited by 13 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. A specific early eluting peak in Bio-Rad Variant II cation-exchange high-performance liquid chromatography (CE-HPLC) for the screening of alpha-thalassaemia in a Chinese population;Pathology;2023-10

2. Application of an optimized interpretation model in capillary hemoglobin electrophoresis for newborn thalassemia screening;International Journal of Laboratory Hematology;2021-09-10

3. Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program;Hemoglobin;2017-11-02

4. A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α⁰-Thalassemia;Acta Haematologica;2017

5. A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia;British Journal of Haematology;2016-02-25