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Volumn 104, Issue 27, 2007, Pages 11346-11351
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Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
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Author keywords
hemoglobinopathies; Complex trait; F cells
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Indexed keywords
HEMOGLOBIN;
PROTEIN MYB;
ADULT;
AGED;
ALLELISM;
ARTICLE;
CHROMOSOME 6Q;
CONTROLLED STUDY;
EUROPEAN AMERICAN;
FETUS;
GENE;
GENE EXPRESSION;
GENETIC ASSOCIATION;
GENETIC TRAIT;
GENETIC VARIABILITY;
GENOTYPE;
HBS1L GENE;
HEMOGLOBINOPATHY;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
QUANTITATIVE TRAIT LOCUS;
ADOLESCENT;
ADULT;
AGED;
CHROMOSOMES, HUMAN, PAIR 6;
DNA, INTERGENIC;
ERYTHROID PROGENITOR CELLS;
FETAL HEMOGLOBIN;
HUMANS;
MIDDLE AGED;
POLYMORPHISM, SINGLE NUCLEOTIDE;
PROTO-ONCOGENE PROTEINS C-MYB;
QUANTITATIVE TRAIT LOCI;
TWIN STUDIES;
VARIATION (GENETICS);
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EID: 34547450531
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.0611393104 Document Type: Article |
Times cited : (264)
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References (29)
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