Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3′ end of the β-globin gene cluster-Reference-Cited by-同舟云学术

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Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3′ end of the β-globin gene cluster

Published:1997-08-04 Issue:3-4 Volume:100 Page:441-445
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Kosteas Theodoros,Palena Antonella,Anagnou N. P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050530.pdf

Cited by 28 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. Establishment and application of a novel method based on single nucleotide polymorphism analysis for detecting β-globin gene cluster deletions;Scientific Reports;2020-10-26

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

3. Diagnosis and prevention of thalassemia;Critical Reviews in Clinical Laboratory Sciences;2013-11

4. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles ofα-thalassemia, 5′ δ-globin BCL11A binding region and 3′ β-globin enhancer;European Journal of Haematology;2013-10-24

5. A Single-Tube Multiplex Gap-Polymerase Chain Reaction for the Detection of Eight β-Globin Gene Cluster Deletions Common in Southeast Asia;Hemoglobin;2012-08

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