Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia-Reference-Cited by-同舟云学术

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Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia

Published:1985-06 Issue:1 Fifth Cooley' Volume:445 Page:159-169
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Ann NY Acad Sci

Author:

FEINGOLD ELISE A.,COLLINS FRANCIS S.,METHERALL JAMES E.,STOECKERT CHRISTIAN J.,WEISSMAN SHERMAN M.,FORGET BERNARD G.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1985.tb17185.x/fullpdf

Reference43 articles.

1. Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia

2. Fetal Haemoglobin Production and the Sickle Gene in the Oases of Eastern Saudi Arabia

3. Restriction endonuclease mapping of the human γ globin gene loci

4. Characterisation of deletions which affect the expression of fetal globin genes in man

Cited by 9 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. β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter;The American Journal of the Medical Sciences;1992-08

2. Prenatal diagnosis of β-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes;Prenatal Diagnosis;1989-09

3. Prenatal diagnosis of beta thalassaemia based on restriction endonuclease analysis of amplified fetal DNA.;Journal of Medical Genetics;1989-06-01

4. Molecular characterization of a novel form of (A ) -thalassemia, deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism;Nucleic Acids Research;1988-07-11

5. Approach to the Diagnosis of β-Thalassaemia by DNA Analysis;Acta Haematologica;1987

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