BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 16628732)

  • 21. Spontaneous mutation of the hemoglobin Leiden (beta 6 or 7 Glu-->0) in a Thai girl.
    Sanguansermsri P; Shimbhu D; Wongvilairat R; Pimsorn C; Sanguansermsri T
    Haematologica; 2003 Dec; 88(12):ECR35. PubMed ID: 14688008
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
    Yi P; Yu F; Huang S; Zhong C; Li Q; Yang Y; Zhang W; Xiao C; Xu X
    Blood Cells Mol Dis; 2008; 41(1):56-9. PubMed ID: 18381244
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.
    Basran RK; Reiss UM; Luo HY; Ware RE; Chui DH
    Pediatr Blood Cancer; 2008 Feb; 50(2):363-6. PubMed ID: 16732578
    [TBL] [Abstract][Full Text] [Related]  

  • 25. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
    Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC
    Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Delta-thalassemia in Cyprus.
    Pavlou E; Phylactides M; Kyrri A; Kalogerou E; Makariou C; Georgiou I; Kleanthous M
    Hemoglobin; 2006; 30(4):455-62. PubMed ID: 16987800
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene.
    Frischknecht H; Dutly F
    Hemoglobin; 2005; 29(2):151-4. PubMed ID: 15921167
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.
    Eng B; Chui DH; Saunderson J; Olivieri NF; Waye JS
    Hum Mutat; 1993; 2(5):375-9. PubMed ID: 8257991
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two new alpha-thalassemia point mutations that are undetectable by biochemical techniques.
    Joly P; Pégourie B; Courby S; Barro C; Besson G; Cohen L; Garcia C; Francina A
    Hemoglobin; 2008; 32(4):411-7. PubMed ID: 18654892
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
    Foulon K; Rochette J; Cadet E
    Hemoglobin; 2007; 31(1):31-7. PubMed ID: 17365003
    [TBL] [Abstract][Full Text] [Related]  

  • 31. C to T transition at the first nucleotide of codon 63 of the beta-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy.
    Suryantoro P; Takeshima Y; Haryanto A; Matsuo M
    Jpn J Hum Genet; 1995 Jun; 40(2):195-201. PubMed ID: 7663000
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].
    Ropero P; González FA; Sánchez J; Armada B; Martí E; Valdés B; Mora A; Villegas A
    Med Clin (Barc); 1997 Mar; 108(10):385-8. PubMed ID: 9139146
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel frameshift mutation (+G) at codons 15/16 in a beta0 thalassaemia gene results in a significant reduction of beta globin mRNA values.
    Mo QH; Li XR; Li CF; He YL; Xu XM
    J Clin Pathol; 2005 Sep; 58(9):923-6. PubMed ID: 16126871
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
    Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations.
    Douna V; Papassotiriou I; Metaxotou-Mavrommati A; Stamoulakatou A; Liapi D; Kampourakis D; Tsilimigaki A; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(4):379-85. PubMed ID: 18654888
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I
    Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hemoglobin S/hemoglobin Osler: a case with 3 beta globin chains. DNA sequence (AAT) proves that Hb Osler is beta 145 Tyr-->Asn.
    Hutt PJ; Donaldson MH; Khatri J; Fairbanks VF; Hoyer JD; Thibodeau SN; Moxness MS; McMorrow LE; Green MM; Jones RT
    Am J Hematol; 1996 Aug; 52(4):305-9. PubMed ID: 8701949
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two independent origins of Hb Dhonburi (Neapolis) [beta 126 (H4) Val-->Gly]: an electrophoretically silent hemoglobin variant.
    Viprakasit V; Chinchang W
    Clin Chim Acta; 2007 Feb; 376(1-2):179-83. PubMed ID: 17007829
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG).
    Luo HY; Tang W; Eung SH; Coad JE; Canfield P; Keller F; Crowell EH; Steinberg MH; Chui DH
    J Clin Pathol; 2005 Oct; 58(10):1110-2. PubMed ID: 16189162
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2.
    Keser I; Kayisli OG; Yesilipek A; Ozes ON; Luleci G
    Hemoglobin; 2001 Nov; 25(4):369-73. PubMed ID: 11791869
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.