BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

729 related articles for article (PubMed ID: 30200838)

  • 1. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Jha AN; Mishra H; Verma HK; Pandey I; Lakkakula BVKS
    Hemoglobin; 2018 Mar; 42(2):84-90. PubMed ID: 30200838
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hb S (
    Azarkeivan A; Cohan N; Niazkar HR; Azizi A; Rad F
    Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb S/
    Belisário AR; Carneiro-Proietti AB; Sabino EC; Araújo A; Loureiro P; Máximo C; Flor-Park MV; Rodrigues DDOW; Ozahata MC; McClure C; Mota RA; Gomes Moura IC; Custer B; Kelly S;
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
    [TBL] [Abstract][Full Text] [Related]  

  • 4. First Report of Compound Heterozygosity for Hb S (
    Ogu UO; Reyes Gil M; Tolu SS; Acharya SA; Minniti CP
    Hemoglobin; 2021 Mar; 45(2):136-139. PubMed ID: 34134586
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
    Dehury S; Meher S; Patel S; Das K; Jana A; Bhattacharya S; Sahoo S; Sarkar B; Mohanty PK
    Hemoglobin; 2019 Mar; 43(2):132-136. PubMed ID: 31190580
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β
    Abdaoui W; Benouareth DE; Djenouni A; Renoux C; Grifi F; Gouri A; Athamnia F; Benalioua M; Joly P
    Hemoglobin; 2019; 43(4-5):223-228. PubMed ID: 31603010
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
    Patel DK; Patel M; Mashon RS; Patel S; Dash PM; Das BS
    Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia.
    Dash PM; Sahu PK; Patel S; Mashon RS; Kharat KR; Mukherjee MB
    Hemoglobin; 2018 Jul; 42(4):236-242. PubMed ID: 30486691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Profiling of 35 Cases of Hb S/Hb E (
    Dehury S; Mohanty PK; Patel S; Meher S; Das K; Purohit P; Sahoo S; Ratha J
    Hemoglobin; 2021 Nov; 45(6):380-386. PubMed ID: 35243949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
    Belhaj Nefissi R; Doggui R; Ouali F; Messaoud T; Gritli N
    Hemoglobin; 2018 Mar; 42(2):96-102. PubMed ID: 30200836
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program.
    Vachhani NA; Vekariya DJ; Colah RB; Kashiyani HN; Nandani SL
    Hemoglobin; 2022 Sep; 46(5):285-289. PubMed ID: 36367309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with β-Thalassemia and Sickle Cell Disease.
    Listì F; Sclafani S; Agrigento V; Barone R; Maggio A; D'Alcamo E
    Hemoglobin; 2018 Mar; 42(2):103-107. PubMed ID: 30200835
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb A
    Orts JA; Zúñiga Á; Bello Y; Fabregat AB; Vicente AI
    Hemoglobin; 2016 Sep; 40(5):335-340. PubMed ID: 27535164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.
    Meher S; Dehury S; Mohanty PK; Patel S; Pattanayak C; Bhattacharya S; Das K; Sarkar B
    Hemoglobin; 2016 Aug; 40(4):270-2. PubMed ID: 27254408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-thalassemia codon 17 (A>T) in a Thai patient.
    Pornprasert S; Panyasai S; Kongthai K; Treesuwan K
    Hemoglobin; 2012; 36(3):265-9. PubMed ID: 22471390
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inherited hemoglobin disorders in Guinea-Bissau, West Africa: a population study.
    Masmas TN; Garly ML; Lisse IM; Rodriques A; Petersen PT; Birgens H
    Hemoglobin; 2006; 30(3):355-64. PubMed ID: 16840226
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 39(3):156-61. PubMed ID: 25806420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [S hemoglobinopathies in Argentina].
    Abreu MS; Peñalver JA
    Medicina (B Aires); 1992; 52(4):341-6. PubMed ID: 1340883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
    Gupta RB; Tiwary RS; Pande PL; Kutlar F; Oner C; Oner R; Huisman TH
    Hemoglobin; 1991; 15(5):441-58. PubMed ID: 1802886
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
    Murad H; Moassas F; Jarjour R; Mukhalalaty Y; Al-Achkar W
    Hemoglobin; 2014; 38(6):390-3. PubMed ID: 25405916
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 37.