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 *

107 related articles for article (PubMed ID: 11939512)

  • 41. Co-existence of the codon 16 (-C) (beta(o)) and codon 10 (C --> A) (beta+) mutations on the same beta-globin gene.
    Colah RB; Nadkarni A; Pawar A; Gorakshakar A; Phanasgaonkar S; Mohanty D
    Hemoglobin; 2003 May; 27(2):133-5. PubMed ID: 12779277
    [No Abstract]   [Full Text] [Related]  

  • 42. Hb Florida: a novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype.
    Weinstein BI; Erramouspe B; Albuquerque DM; Oliveira DM; Kimura EM; Costa FF; Sonati MF
    Am J Hematol; 2006 May; 81(5):358-60. PubMed ID: 16628732
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A 65 bp duplication/insertion in exon II of the beta globin gene causing beta0-thalassemia.
    Frischknecht H; Dutly F
    Haematologica; 2007 Mar; 92(3):423-4. PubMed ID: 17339197
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Human alpha2-globin nonsense-mediated mRNA decay induced by a novel alpha-thalassaemia frameshift mutation at codon 22.
    Pereira FJ; do Céu Silva M; Picanço I; Seixas MT; Ferrão A; Faustino P; Romão L
    Br J Haematol; 2006 Apr; 133(1):98-102. PubMed ID: 16512835
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Rare beta-thalassaemia mutations in Asian indians.
    Varawalla NY; Old JM; Weatherall DJ
    Br J Haematol; 1991 Dec; 79(4):640-4. PubMed ID: 1772786
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
    Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
    Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A new beta-thalassemia allele, codon 26 (GAG-->GTAG), found in a Japanese.
    Hattori Y; Okayama N; Ohba Y; Yamashiro Y; Yamamoto K; Yamamoto K; Koyama S; Sawada U
    Hemoglobin; 1998 Jan; 22(1):79-82. PubMed ID: 9494052
    [No Abstract]   [Full Text] [Related]  

  • 48. Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish cases.
    Bozdogan ST; Unsal C; Erkman H; Genc A; Yuregir OO; Muslumanoglu MH; Aslan H
    Hemoglobin; 2012; 36(3):283-8. PubMed ID: 22385009
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The clinical severity of beta-thalassemia mutations in West Malaysia.
    George E
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():225-8. PubMed ID: 8629111
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R; Nadkarni A; Gorakshakar A; Phanasgaonkar S; Surve R; Subramaniam PG; Bondge N; Pujari K; Ghosh K; Mohanty D
    Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A novel 105 basepair deletion causing beta(0)-thalassemia in members of a Thai family.
    Nopparatana C; Saechan V; Nopparatana C; Pornpatkul M; Panich V; Fukumaki Y
    Am J Hematol; 1999 May; 61(1):1-4. PubMed ID: 10331503
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Molecular basis of antithrombin type I deficiency: the first large in-frame deletion and two novel mutations in exon 6.
    Emmerich J; Chadeuf G; Alhenc-Gelas M; Gouault-Heilman M; Toulon P; Fiessinger JN; Aiach M
    Thromb Haemost; 1994 Oct; 72(4):534-9. PubMed ID: 7878627
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.
    Wang W; Kham SK; Yeo GH; Quah TC; Chong SS
    Clin Chem; 2003 Feb; 49(2):209-18. PubMed ID: 12560342
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A new insertion mutation in the beta-globin gene [codons 45/46 (+A)] resulting in a beta-thalassemia minor phenotype.
    Cornut G; Weng X; Robin L; Lavoie C; Marchand S; Soulières D
    Hemoglobin; 2007; 31(3):393-5. PubMed ID: 17654079
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The beta+-IVS-I-6 (T-->C) mutation accounts for half of the thalassemia chromosomes in the Palestinian populations of the mountain regions.
    El-Latif MA; Filon D; Rund D; Oppenheim A; Kanaan M
    Hemoglobin; 2002 Feb; 26(1):33-40. PubMed ID: 11939510
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Japanese beta zero-thalassemia: molecular characterization of a novel insertion causing a stop codon.
    Oshima K; Harano T; Harano K
    Am J Hematol; 1996 May; 52(1):39-41. PubMed ID: 8638609
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Codon 4 ACT-->ACA, codon 5 CCT-->TCT, and codon 6 GAG-->TAG mutations in cis position: a form of thalassemia trait.
    Agarwal S; Wei L; Hattori Y; Agarwal SS
    Am J Hematol; 1997 Nov; 56(3):187-8. PubMed ID: 9371533
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh.
    Aziz A; Das SA; Khan WA; Sadiya S; Banu B; Sarwardi G; Luna RZ
    Hemoglobin; 2017; 41(4-6):311-313. PubMed ID: 29313434
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A new β-thalassemia deletion mutation [codon 36 (-C)] observed in a Chinese woman.
    Huang H; Xu L; Lin N; Xu J; He D; Li Y; Zheng L; Liu H; Lin Y
    Hemoglobin; 2010; 34(6):599-603. PubMed ID: 21077770
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel beta-thalassaemia mutation in the 5' untranslated region of the beta-globin gene.
    Athanassiadou A; Papachatzopoulou A; Zoumbos N; Maniatis GM; Gibbs R
    Br J Haematol; 1994 Oct; 88(2):307-10. PubMed ID: 7803275
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.