Differentiation of homozygous hemoglobin E from compound heterozygous hemoglobin E-β0-thalassemia by hemoglobin E mutation analysis
- 31 May 1992
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 120 (5) , 775-779
- https://doi.org/10.1016/s0022-3476(05)80247-1
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- RAPID DETECTION OF βs DNA FROM GUTHRIE CARDS BY CHROMOGENIC PROBESThe Lancet, 1989
- Polymerase chain reaction amplification applied to the determination of β‐like globin gene cluster haplotypesAmerican Journal of Hematology, 1989
- Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide ProbesNew England Journal of Medicine, 1988
- GUTHRIE CARDS FOR DETECTION OF POINT MUTATIONS IN PHENYLKETONURIAThe Lancet, 1988
- [21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reactionPublished by Elsevier ,1987
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Identification of β Vartant Hemoglobins by DNA Restriction Endonuclease MappingHemoglobin, 1984
- Anemia and hemoglobinopathies in Southeast Asian refugee childrenThe Journal of Pediatrics, 1983
- Homozygous hemoglobin E mimics β-thalassemia minor without anemia or hemolysis: Hematologic, functional, and biosynthetic studies of first north American casesAmerican Journal of Hematology, 1980
- Hb Henri Mondor: β26 (B8) Glu → Val: A variant with a substitution localized at the same position as that of HbE β26 Glu → LysFEBS Letters, 1976