These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

377 related articles for article (PubMed ID: 6359893)

  • 21. alpha-globin gene deletions associated with Hb J Tongariki.
    Bowden DK; Pressley L; Higgs DR; Clegg JB; Weatherall DJ
    Br J Haematol; 1982 Jun; 51(2):243-9. PubMed ID: 6979350
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Secondary and tertiary structure aberration of alpha globin chain in haemoglobin Q-India disorder.
    Wiwanitkit V
    Indian J Pathol Microbiol; 2006 Oct; 49(4):491-4. PubMed ID: 17183835
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL; Versteegh FG; van Leer EH; Starreveld JS; Kok PJ; van Rooijen-Nijdam I; van Delft P; Zanella-Cleon I; Becchi M; Wajcman H; Giordano PC
    Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg).
    Weiss I; Cash FE; Coleman MB; Pressley A; Adams JG; Sanguansermsri T; Liebhaber SA; Steinberg MH
    Blood; 1990 Dec; 76(12):2630-6. PubMed ID: 2265255
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
    Luo HY; Heeney M; Wang WC; Eung SH; Ware RE; Steinberg MH; Chui DH
    Am J Hematol; 2006 May; 81(5):361-5. PubMed ID: 16628724
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular genetics of human hemoglobin synthesis.
    Forget BG
    Ann Intern Med; 1979 Oct; 91(4):605-16. PubMed ID: 384860
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic defects in the thalassemias.
    Bank A
    Curr Top Hematol; 1985; 5():1-23. PubMed ID: 3882340
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [The hemoglobinopathies due to a disturbance of hemoglobin synthesis].
    Labie D; Dreyfus JC
    Nouv Rev Fr Hematol; 1971; 11(1):83-93. PubMed ID: 4252108
    [No Abstract]   [Full Text] [Related]  

  • 32. Scanning method to identify the molecular heterogeneity of delta-globin gene especially in delta-thalassemias: detection of three novel substitutions in the promoter region of the gene.
    Papadakis M; Papapanagiotou E; Loutradi-Anagnostou A
    Hum Mutat; 1997; 9(5):465-72. PubMed ID: 9143928
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.
    Ropero P; Villegas A; Martínez M; Ataulfo González Fernández F; Benavente C; Mateo M
    Ann Hematol; 2005 Sep; 84(9):584-7. PubMed ID: 15977037
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer.
    Sangkitporn SK; Eksiri L; Sangnoi A; Duangruang S; Dumbua A; Rattanakittisophon K; Sangkitporn S
    Int J Lab Hematol; 2009 Oct; 31(5):521-7. PubMed ID: 18498386
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Laboratory investigation of hemoglobinopathies and thalassemias: review and update.
    Clarke GM; Higgins TN
    Clin Chem; 2000 Aug; 46(8 Pt 2):1284-90. PubMed ID: 10926923
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.
    De Angioletti M; Lacerra G; Gaudiano C; Mastrolonardo G; Pagano L; Mastrullo L; Masciandaro S; Carestia C
    Hum Mutat; 2002 Nov; 20(5):358-67. PubMed ID: 12402333
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Globin gene deletion in HPFH, delta (o) beta (o) thalassaemia and Hb Lepore disease.
    Ottolenghi S; Giglioni B; Comi P; Gianni AM; Polli E; Acquaye CT; Oldham JH; Masera G
    Nature; 1979 Apr; 278(5705):654-7. PubMed ID: 450068
    [No Abstract]   [Full Text] [Related]  

  • 38. Hemoglobin variants in Cyprus.
    Kyrri AR; Felekis X; Kalogerou E; Wild BJ; Kythreotis L; Phylactides M; Kleanthous M
    Hemoglobin; 2009; 33(2):81-94. PubMed ID: 19373583
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel beta-globin mutation, beta Durham-NC [beta 114 Leu-->Pro], produces a dominant thalassemia-like phenotype.
    de Castro CM; Devlin B; Fleenor DE; Lee ME; Kaufman RE
    Blood; 1994 Feb; 83(4):1109-16. PubMed ID: 8111050
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG; Bhanushali AA; Dedhia P; Jeswani KD; Dayanand S; Dasgupta A; Das BR
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.