BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

321 related articles for article (PubMed ID: 2274839)

  • 1. [Analysis of a program for atypical familial microcytosis. Molecular basis of alpha-thalassemia].
    Villegas Martínez A
    Sangre (Barc); 1990 Aug; 35(4):277-88. PubMed ID: 2274839
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.
    Efremov GD
    Haematologica; 1990; 75 Suppl 5():31-41. PubMed ID: 2086380
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alpha thalassaemia in two Spanish families.
    Villegas A; Calero F; Vickers MA; Ayyub H; Higgs DR
    Eur J Haematol; 1990 Feb; 44(2):109-15. PubMed ID: 2318293
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Screening for alpha-thalassemia using DNA analysis].
    Beris P; Grossiord D; Hochmann A; Zhu L; Miescher PA
    Schweiz Med Wochenschr; 1988 Oct; 118(42):1538-41. PubMed ID: 3201208
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular genetic studies in alpha-thalassemia].
    de Korte D; Cuypers HT; de Klein A; Winkel I; Vuil H; Roos D
    Ned Tijdschr Geneeskd; 1992 May; 136(18):872-5. PubMed ID: 1350329
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
    Sura T; Busabaratana M; Youngcharoen S; Wisedpanichkij R; Viprakasit V; Trachoo O
    Eur J Haematol; 2007 Sep; 79(3):251-4. PubMed ID: 17655700
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia.
    Wainscoat JS; Bell JI; Old JM; Weatherall DJ; Furbetta M; Galanello R; Cao A
    Mol Biol Med; 1983 Jul; 1(1):1-10. PubMed ID: 6092822
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
    Adams JG; Boxer LA; Baehner RL; Forget BG; Tsistrakis GA; Steinberg MH
    J Clin Invest; 1979 May; 63(5):931-8. PubMed ID: 447835
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.
    Akerman BR; Fujiwara TM; Lancaster GA; Morgan K; Scriver CR
    Am J Med Genet; 1990 May; 36(1):76-84. PubMed ID: 2333910
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Atypical familial microcytosis: a familial and genetic study].
    Remacha AF; del Río E; Baiget M
    Med Clin (Barc); 1998 Feb; 110(5):183-5. PubMed ID: 9547723
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China.
    Xiong F; Sun M; Zhang X; Cai R; Zhou Y; Lou J; Zeng L; Sun Q; Xiao Q; Shang X; Wei X; Zhang T; Chen P; Xu X
    Clin Genet; 2010 Aug; 78(2):139-48. PubMed ID: 20412082
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
    Fucharoen S; Fucharoen G; Sae-ung N; Sanchaisuriya K
    Blood Cells Mol Dis; 2007; 39(2):195-8. PubMed ID: 17587614
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Different molecular defects of G gamma (A gamma delta beta)o-thalassaemia in Thailand.
    Fucharoen S; Winichagoon P; Chaicharoen S; Wasi P
    Eur J Haematol; 1987 Aug; 39(2):154-60. PubMed ID: 2889616
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
    Bowden DK; Hill AV; Higgs DR; Oppenheimer SJ; Weatherall DJ; Clegg JB
    J Clin Invest; 1987 Jan; 79(1):39-43. PubMed ID: 3793931
    [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 17.