Hb A2-MONREALE [δ146(HC3)His → Arg], A NOVEL δ CHAIN VARIANT DETECTED IN WEST SICILY-Reference-Cited by-同舟云学术

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Hb A2-MONREALE [δ146(HC3)His → Arg], A NOVEL δ CHAIN VARIANT DETECTED IN WEST SICILY

Published:2002-01 Issue:1 Volume:26 Page:1-5
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

De Angioletti Maria,Di Girgenti Caterina,Messineo Rosalia,Capra Marcello,Carestia Clementina

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120002934

Reference6 articles.

1. Hpal, HindIII, and BamHI polymorphisms 3′ of the human β-globin gene can be detected by a single polymerase chain reaction amplification product

2. Rapid and non-radioactive prenatal diagnosis of β thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)

3. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster

4. Hemoglobin cochin-port-royal: Consequences of the replacement of the β chain C-terminal by an arginine

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. A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA1c;International Journal of Hematology;2012-04-08

2. Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation;Hemoglobin;2007-01

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