Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutations

Author:

Galanello R.,Paglietti M. E.,Addis M.,Melis M. A.,Tuveri T.,Furbetta M.,Cao A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. Nonrandom association of polymorphic restriction sites in β-globin gene cluster;Antonarakis;Proc. Natl. Acad. Sci. USA,1982

2. βthalassemia trait in Sardinia;Galanello;Hemoglobin,1979

3. Hematological phenotype of carriers of deletion α-thalassemia according to the α-globin genotype;Galanello;Haematologica,1985

4. DNA analysis in the diagnosis of hemoglobin disorders;Goossens;Methods Enzymol.,1981

5. Microchromatography of haemoglobins. III. A simplified method for the determination of haemoglobin A2;Huisman;J. Lab. Clin. Med.,1975

Cited by 5 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. Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation;Blood Cells, Molecules, and Diseases;2017-05

2. Screening for thalassemia;Obstetrics and Gynecology Clinics of North America;2002-06

3. Genetic Modifying Factors in β-Thalassemia;Clinical Chemistry and Laboratory Medicine;2000-01-05

4. 8 Prenatal diagnosis and screening of the haemoglobinopathies;Baillière's Clinical Haematology;1998-03

5. Population-based genetic screening;Current Opinion in Genetics & Development;1991-06

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