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Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Chaturvedi, Shruti; Bhatnagar, Pallav; Bean, Christopher J; Steinberg, Martin H; Milton, Jaqueline N; Casella, James F; Barron-Casella, Emily; Arking, Dan E; DeBaun, Michael R.
Affiliation
  • Chaturvedi S; Division of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Bhatnagar P; McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD.
  • Bean CJ; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA.
  • Steinberg MH; Department of Medicine.
  • Milton JN; Department of Pediatrics, and.
  • Casella JF; Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA.
  • Barron-Casella E; Department of Biostatistics, Boston University School of Public Health, Boston, MA.
  • Arking DE; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
  • DeBaun MR; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
Blood ; 130(5): 686-688, 2017 08 03.
Article in En | MEDLINE | ID: mdl-28584135
Subject(s)
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Full text: 1 Database: MEDLINE Main subject: Arterial Occlusive Diseases / Genetic Variation / Chromosomes, Human, Pair 4 / Polymorphism, Single Nucleotide / Epistasis, Genetic / Acute Pain / Anemia, Sickle Cell Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Blood Year: 2017 Type: Article Affiliation country: Tunisia
Fulltext
Add to My VHL
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Full text: 1 Database: MEDLINE Main subject: Arterial Occlusive Diseases / Genetic Variation / Chromosomes, Human, Pair 4 / Polymorphism, Single Nucleotide / Epistasis, Genetic / Acute Pain / Anemia, Sickle Cell Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Blood Year: 2017 Type: Article Affiliation country: Tunisia