Hpal polymorphic site 3′ of the human β-globin gene is inside a repetitive sequence and cannot be ascertained by polymerase chain reaction-Reference-Cited by-同舟云学术

Hpal polymorphic site 3′ of the human β-globin gene is inside a repetitive sequence and cannot be ascertained by polymerase chain reaction

Published:1992-03 Issue:3 Volume:39 Page:226-227
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Wang Xiuhua,Bouhassira Eric E.

Publisher

Wiley

Subject

Hematology

Reference5 articles.

1. , , , , , : Known and potential sources for epistatic effects in sickle cell anemia. In (eds): “Sickle Cell Disease (ann NY Acad Sci Vol 565)” New York: New York Academy of Sciences, 1989, pp 228–238.

2. βS-Gene-Cluster Haplotypes in Sickle Cell Anemia

3. Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes

4. KpnI families of long, interspersed repetitive DNAs associated with the human β-globin gene cluster

5. Sequence analysis of a Kpnl family member near the 3′ end of human β-globin gene

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1. β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ⁰-Thalassemia and Their Association with Clinical and Hematological Features;Acta Haematologica;2010

2. Beta-globin haplotypes from blood spots for follow-up of newborn hemoglobinopathy screening;American Journal of Hematology;1997-01

3. Haplotypes of the human β-like globin gene cluster: Analyzing the 3′ Hpa I polymorphic site by long distance PCR;American Journal of Hematology;1995-09

4. Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia;American Journal of Hematology;1995-03

5. Hpal, HindIII, and BamHI polymorphisms 3′ of the human β-globin gene can be detected by a single polymerase chain reaction amplification product;American Journal of Hematology;1994-11