High-density SNP genotyping to define β-globin locus haplotypes

Blood Cells, Molecules, and Diseases

Volumn 42, Issue 1, 2009, Pages 16-24

  Liu, Li ^a   Muralidhar, Shalini ^a   Singh, Manisha ^a   Sylvan, Caprice ^b   Kalra, Inderdeep S ^a   Quinn, Charles T ^c   Onyekwere, Onyinye C ^b   Pace, Betty S ^a  

^a UNIVERSITY OF TEXAS AT DALLAS   (United States)

^b HOWARD UNIVERSITY   (United States)

^c UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

locus; Haplotype; Haploview; Sickle cell disease; Single nucleotide polymorphism

Indexed keywords

BETA GLOBIN; HEMOGLOBIN A; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

ARTICLE; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN EXPERIMENT; NORMAL HUMAN; PRIORITY JOURNAL; REGULATOR GENE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM;

AFRICAN AMERICANS; ANEMIA, SICKLE CELL; BETA-GLOBINS; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENOTYPE; HAPLOTYPES; HEMOGLOBIN A; HEMOGLOBIN, SICKLE; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 57949086484     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2008.07.002     Document Type: Article

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