Genetic regulation of ? gene expression: Study of the interaction of ?-thalassemia with heterocellular HPFH-Reference-Cited by-同舟云学术

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Genetic regulation of ? gene expression: Study of the interaction of ?-thalassemia with heterocellular HPFH

Published:1981-07 Issue:4 Volume:57 Page:371-375
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Soummer A. M.,Testa U.,Dujardin P.,Guerrasio A.,Henri A.,Gazaix M.,Riou J.,Rochant H.,Beuzard Y.,Rosa J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00281687.pdf

Reference27 articles.

1. Alter BP, Goff SC, Efremov GD, Gravely ME, Huisman TH (1980) Globin chain electrophoresis: a new approach to the determination of the G?/A? ratio in fetal haemoglobin and to studies of globin synthesis. Br J Haematol 44:527?534

2. Basset P, Beuzard Y, Garel MC, Rosa J (1978) Isoelectric focusing of human hemoglobins. Its application to screening, to the characterization of 70 variants and to the study of modified fractions of normal hemoglobins. Blood 51:971?982

3. Betke K, Marti HR, Schlicht I (1959) Estimation of small percentage of foetal haemoglobin. Nature 184:1877?1888

4. Beutler E, West C, Blume KG (1976) The removal of leukocytes and platelets from whole blood. J Lab Clin Med 88:328?333

5. Beuzard Y, Molko F, Cacheleux J, Tsapis A (1978) Evaluation of the pool of ? chains and study of the dissociation of the hemoglobins into monomers. In: Caughey W (ed) Biochemical and clinical aspects of hemoglobin abnormalities. Academic Press, New York, p 227

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1. The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab;Scandinavian Journal of Haematology;2009-04-24

2. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age;Blood;1995-02-15

3. γ-mRNA and Hb F levels in β-thalassaemia;British Journal of Haematology;1994-10

4. Report of the committee on clinical disorders and chromosomal deletion syndromes;Cytogenetic and Genome Research;1990

5. The Emerging Complexity of Genetic Control of Persistent Fetal Hemoglobin Biosynthesis in Adults;Annals of the New York Academy of Sciences;1989-07

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