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PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, pp. e92506 - e92506
Background: Genetic variation at loci influencing adult levels of HbF have been shown to modify the clinical course of sickle cell disease (SCD). Data on this... 
GENETIC-VARIATION | POPULATION | ANEMIA PATIENTS | RISK-FACTORS | ACUTE CHEST SYNDROME | MULTIDISCIPLINARY SCIENCES | FETAL-HEMOGLOBIN | DISEASE | HAPLOTYPES | BETA-THALASSEMIA | GENOME-WIDE ASSOCIATION | Prognosis | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | Hospitalization - statistics & numerical data | Proto-Oncogene Proteins c-myb - genetics | Male | Erythrocytes, Abnormal - metabolism | GTP-Binding Proteins - genetics | Young Adult | Haplotypes - genetics | Anemia, Sickle Cell - epidemiology | Polymerase Chain Reaction | Adult | Female | Nuclear Proteins - genetics | Child | Peptide Elongation Factors - genetics | Fetal Hemoglobin - metabolism | African Americans - genetics | HSP70 Heat-Shock Proteins - genetics | Carrier Proteins - genetics | Erythrocytes, Abnormal - pathology | Phenotype | Cameroon - epidemiology | Polymorphism, Restriction Fragment Length | Anemia, Sickle Cell - metabolism | Adolescent | Polymorphism, Single Nucleotide - genetics | Anemia, Sickle Cell - genetics | Medical research | Sickle cell anemia | African Americans | Medicine, Experimental | Medical records | Hemoglobin | Hydroxyurea | Research | Comparative analysis | Blood transfusion | Haplotypes | Health sciences | Transfusion | Single-nucleotide polymorphism | Blood | Gene sequencing | Ethics | Demographics | Genetic analysis | Chromosome 11 | Genetics | Electrophoresis | Population | Mathematical models | Sickle cell disease | Chromosomes | Public health | Parasitology | Statistical analysis | Hematology | Capillary electrophoresis | Fetuses | Genetic diversity | Minority & ethnic groups | Patients | Loci | HBB gene | Homozygotes | Medicine | Statistical models | Infectious diseases | Genotyping | Gene frequency | Influence | Mutation | Index Medicus
Journal Article
Journal Article
Nature, ISSN 0028-0836, 2010, Volume 467, Issue 7313, pp. 318 - 322
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2013, Volume 8, Issue 2, pp. e54626 - e54626
Human genome sequencing has resulted in a great body of data, including a stunningly large number of single nucleotide polymorphisms (SNPs) with unknown... 
ELEMENTS | FLANKING SEQUENCES | GLOBIN GENE | ATA BOX | DNA | MULTIDISCIPLINARY SCIENCES | TRIOSEPHOSPHATE ISOMERASE | MUTATION | CONSENSUS | BETA-THALASSEMIA | PRENATAL-DIAGNOSIS | Cytochrome P-450 CYP2A6 | Superoxide Dismutase - genetics | Disease - genetics | Humans | Aryl Hydrocarbon Hydroxylases - genetics | Computational Biology | Interleukin-1beta - genetics | Mannose-Binding Lectin - genetics | Promoter Regions, Genetic - genetics | TATA-Box Binding Protein - metabolism | Globins - genetics | Nitric Oxide Synthase Type II - genetics | Models, Biological | TATA Box - genetics | Protein Binding | Polymorphism, Single Nucleotide | Superoxide Dismutase-1 | Medical research | Lung cancer | Genes | Genomics | Genomes | Prothrombin complex concentrate | Analysis | Hemophilia | Medicine, Experimental | Genetic aspects | Single nucleotide polymorphisms | Nucleotide sequencing | Protein binding | DNA sequencing | Myocardial infarction | Transcription factors | Single-nucleotide polymorphism | Multivariate analysis | Sclerosis | Boxes | Gene sequencing | Proteins | Genetics | Tata box | Deoxyribonucleic acid--DNA | Genetic disorders | Immune response | Health risks | Amyotrophic lateral sclerosis | Thalassemia | Thrombophlebitis | Gene expression | Equilibrium | Diseases | Immune systems | TATA-binding protein | Cellular biology | Correlation analysis | Electrophoretic mobility | Predictions | Lectins | Affinity | Infarction | Mutation | Molecular biology | Cancer | Index Medicus | Deoxyribonucleic acid
Journal Article
American Journal of Hematology, ISSN 0361-8609, 07/2013, Volume 88, Issue 7, pp. 571 - 576
Journal Article
Cell, ISSN 0092-8674, 04/2018, Volume 173, Issue 2, pp. 430 - 442.e17
Journal Article