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: 3756105)

  • 1. Organization of the zeta-alpha genes in Chinese.
    Chan V; Chan TK; Cheng MY; Kan YW; Todd D
    Br J Haematol; 1986 Sep; 64(1):97-105. PubMed ID: 3756105
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of a newly discovered alpha-thalassaemia-1 in two Spanish patients with Hb H disease.
    Gonzalez-Redondo JM; Diaz-Chico JC; Malcorra-Azpiazu JJ; Balda-Aguirre MI; Huisman TH
    Br J Haematol; 1988 Dec; 70(4):459-63. PubMed ID: 3219296
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene.
    Higgs DR; Pressley L; Old JM; Hunt DM; Clegg JB; Weatherall DJ; Serjeant GR
    Lancet; 1979 Aug; 2(8137):272-6. PubMed ID: 88608
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of an extensive zeta-alpha globin gene deletion in a Chinese individual.
    Waye JS; Eng B; Chui DH
    Br J Haematol; 1992 Mar; 80(3):378-80. PubMed ID: 1581218
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The risk of alpha-thalassaemia in offspring of beta-thalassaemia carriers in Hong Kong.
    Lam YH; Ghosh A; Tang MH; Chan V
    Prenat Diagn; 1997 Aug; 17(8):733-6. PubMed ID: 9267896
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.
    Fei YJ; Liu JC; Jogessar VB; Westermeyer KR; Bridgemohan R; Huisman TH
    Acta Haematol; 1992; 87(1-2):11-5. PubMed ID: 1585766
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of a new alpha zero thalassaemia defect in the South African population.
    Vandenplas S; Higgs DR; Nicholls RD; Bester AJ; Mathew CG
    Br J Haematol; 1987 Aug; 66(4):539-42. PubMed ID: 3663510
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular basis of alpha thalassaemia in a South African population.
    Mathew CG; Rousseau J; Rees JS; Harley EH
    Br J Haematol; 1983 Sep; 55(1):103-11. PubMed ID: 6309210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation.
    Yüregir GT; Aksoy K; Cürük MA; Dikmen N; Fei YJ; Baysal E; Huisman TH
    Br J Haematol; 1992 Apr; 80(4):527-32. PubMed ID: 1581238
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The triplicated alpha gene locus and beta thalassaemia.
    Kanavakis E; Metaxotou-Mavromati A; Kattamis C; Wainscoat JS; Wood WG
    Br J Haematol; 1983 Jun; 54(2):201-7. PubMed ID: 6189508
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.
    Gurgey A; Kayin S; Kansu E; Altay C
    J Med Genet; 1985 Jun; 22(3):213-21. PubMed ID: 2409284
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characteristics and distribution of beta thalassemia haplotypes in South China.
    Chan V; Chan TK; Cheng MY; Leung NK; Kan YW; Todd D
    Hum Genet; 1986 May; 73(1):23-6. PubMed ID: 3011644
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alpha-thalassaemia and globin gene rearrangements in French Polynesia.
    Philippon G; Martinson JJ; Rugless MJ; Moulia-Pelat JP; Plichart R; Roux JF; Martin PM; Clegg JB
    Eur J Haematol; 1995 Sep; 55(3):171-7. PubMed ID: 7672089
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis of a program for atypical familial microcytosis. Molecular basis for alpha-thalassemia. GEHBTA].
    Sangre (Barc); 1990 Apr; 35(2):102-13. PubMed ID: 2363092
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Thalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia.
    Wainscoat JS; Kanavakis E; Wood WG; Letsky EA; Huehns ER; Marsh GW; Higgs DR; Clegg JB; Weatherall DJ
    Br J Haematol; 1983 Mar; 53(3):411-6. PubMed ID: 6297530
    [TBL] [Abstract][Full Text] [Related]  

  • 16. BamH I polymorphism in the Chinese: its potential usefulness in prenatal diagnosis of beta thalassaemia.
    Chan V; Leung NK; Chan TK; Ghosh A; Kan YW; Todd D
    Br Med J (Clin Res Ed); 1984 Oct; 289(6450):947-8. PubMed ID: 6091839
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian family.
    Fortina P; Dianzani I; Serra A; Gottardi E; Saglio G; Farinasso L; Piga A; Gabutti V; Camaschella C
    Br J Haematol; 1991 Aug; 78(4):529-34. PubMed ID: 1911344
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion.
    Chui DH; Wong SC; Chung SW; Patterson M; Bhargava S; Poon MC
    N Engl J Med; 1986 Jan; 314(2):76-9. PubMed ID: 3941693
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.
    Traeger-Synodinos J; Tzetis M; Kanavakis E; Metaxotou-Mavromati A; Kattamis C
    Br J Haematol; 1991 Oct; 79(2):302-5. PubMed ID: 1720325
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
    So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC
    Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.