Diagnosis of the β0Thalassemia Trait at Birth-Reference-Cited by-同舟云学术

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Diagnosis of the β0Thalassemia Trait at Birth

Published:1981-01 Issue:3 Volume:5 Page:217-229
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Furbetta M.,Angius A.,Tuveri T.,Rosatelli C.,Scalas M. T.,Ximenes A.,Falchi A. M.,Cao A.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268108997546

Reference18 articles.

1. Beta Thalassemia Trait: Detection at Birth

2. Gamma-Beta Thalassemia: A Cause of Hemolytic Disease of the Newborn

3. Successful Application of Prenatal Diagnosis in a Pregnancy at Risk for Homozygous β-Thalassemia

4. DIAGNOSIS OF BETA THALASSAEMIA IN THE NEWBORN BY MEANS OF HAEMOGLOBIN SYNTHESIS

5. Prenatal Diagnosis of Hemoglobinopathies: Detection of α-Thalassemia Trait and of Sickle Cell DiseaseIn Utero

Cited by 3 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. Alpha thalassaemia in Sardinian newborns;British Journal of Haematology;1984-10

2. Developmental Pattern of β-Chain Production at Midtrimester Pregnancy in Sardlnlan β°-Thalassemia Heterozycotes;Hemoglobin;1984-01

3. Analysis of rates of globin synthesis in normal human fetuses and neonates and in twins;American Journal of Hematology;1982-04

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