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Journal Abstract Search

803 related items for PubMed ID: 10791557

  • 1. Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.
    Ashley-Koch A, Yang Q, Olney RS.
    Am J Epidemiol; 2000 May 01; 151(9):839-45. PubMed ID: 10791557
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  • 2. Molecular characteristics of pediatric patients with sickle cell anemia and stroke.
    Sarnaik SA, Ballas SK.
    Am J Hematol; 2001 Jul 01; 67(3):179-82. PubMed ID: 11391715
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  • 4. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS.
    Serjeant GR.
    Expert Rev Hematol; 2022 Feb 01; 15(2):107-116. PubMed ID: 35143361
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  • 5. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A, Kutlar F, McKie K, Addington A, Elam D, Holley L, Clair B, Kutlar A.
    Eur J Haematol; 2005 Aug 01; 75(2):150-5. PubMed ID: 16004608
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  • 6. Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola.
    Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M.
    Hemoglobin; 2019 May 01; 43(3):149-154. PubMed ID: 31394941
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  • 8. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
    Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wajcman H, Fabry ME, Nagel RL.
    Proc Natl Acad Sci U S A; 1985 Apr 01; 82(7):2111-4. PubMed ID: 2580306
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  • 9. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age.
    Chang YC, Smith KD, Moore RD, Serjeant GR, Dover GJ.
    Blood; 1995 Feb 15; 85(4):1111-7. PubMed ID: 7531513
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  • 10. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Feb 15; 39(3):156-61. PubMed ID: 25806420
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  • 11. β-globin gene cluster haplotypes in sickle cell patients from Panamá.
    Rusanova I, Cossio G, Moreno B, Javier Perea F, De Borace RG, Perea M, Escames G, Acuña-Castroviejo D.
    Am J Hum Biol; 2011 Feb 15; 23(3):377-80. PubMed ID: 21387457
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  • 12. Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia.
    Al-Ali AK, Alsulaiman A, Alzahrani AJ, Obeid OT, Vatte CB, Cyrus C, Alnafie AN, Alali RA, Alfarhan M, Mozeleski B, Steinberg MH.
    Hemoglobin; 2020 Mar 15; 44(2):78-81. PubMed ID: 32448003
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  • 14. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Mar 15; 36(4):333-42. PubMed ID: 22686351
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  • 15. Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia.
    Hattori Y, Kutlar F, Kutlar A, McKie VC, Huisman TH.
    Hemoglobin; 1986 Mar 15; 10(6):623-42. PubMed ID: 2435679
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  • 16. Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab.
    Torres LS, Okumura JV, Belini-Júnior É, Oliveira RG, Nascimento PP, Silva DG, Lobo CL, Oliani SM, Bonini-Domingos CR.
    Hemoglobin; 2016 Sep 15; 40(5):356-358. PubMed ID: 27535451
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  • 17. Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India.
    Mukherjee MB, Lu CY, Ducrocq R, Gangakhedkar RR, Colah RB, Kadam MD, Mohanty D, Nagel RL, Krishnamoorthy R.
    Am J Hematol; 1997 Jun 15; 55(2):104-9. PubMed ID: 9209006
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  • 19. A novel sickle hemoglobin: hemoglobin S-south end.
    Luo HY, Adewoye AH, Eung SH, Skelton TP, Quillen K, McMahon L, Steinberg MH, Chui DH.
    J Pediatr Hematol Oncol; 2004 Nov 15; 26(11):773-6. PubMed ID: 15543018
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  • 20. The population dynamics of hemoglobins A, A2, F and S in the context of the hemoglobinopathies HbS and α-thalassemia in Kenyan infants.
    Macharia AW, Uyoga S, Ndila C, Nyutu G, Makale J, Tendwa M, Nyatichi E, Ojal J, Atkinson S, Williams TN.
    Haematologica; 2019 May 15; 104(5):e184-e186. PubMed ID: 30467202
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