Identification of the -92 (C→T) Mutation by the Amplification Refractory Mutation Sym in Southern Italy-Reference-Cited by-同舟云学术

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Identification of the -92 (C→T) Mutation by the Amplification Refractory Mutation Sym in Southern Italy

Published:1995-01 Issue:5 Volume:19 Page:307-310
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Pagano L.,Desicato S.,Viola A.,Rosa C. De,Fioretti G.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269509005820

Reference8 articles.

1. The β- and δ-Thalassemia Repository (Seventh Edition)

2. A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia

3. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

4. Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK

Cited by 4 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. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

2. First Report of β-Thalassemia Intermedia in a Patient Compound Heterozygous for –92 (C>T) and Codons 36/37 (–T) Mutations;Hemoglobin;2018-06-12

3. Thalassaemia screening and confirmation of carriers in parents;Best Practice & Research Clinical Obstetrics & Gynaecology;2017-02

4. THE LABORATORY DIAGNOSIS OF HAEMOGLOBINOPATHIES;British Journal of Haematology;1998-06

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