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 *

104 related articles for article (PubMed ID: 3337900)

  • 1. The polyadenylation site mutation in the alpha-globin gene cluster.
    Thein SL; Wallace RB; Pressley L; Clegg JB; Weatherall DJ; Higgs DR
    Blood; 1988 Feb; 71(2):313-9. PubMed ID: 3337900
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
    Traeger-Synodinos J; Kanavakis E; Tzetis M; Kattamis A; Kattamis C
    Am J Hematol; 1993 Nov; 44(3):162-7. PubMed ID: 8213764
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.
    Jassim N; Al-Arrayed S; Gerard N; Al-Mukharraq H; Al-Ajami A; Ramasawmy R; Krishnamoorthy R
    Hemoglobin; 1999 Aug; 23(3):213-20. PubMed ID: 10490133
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemia.
    Harteveld CL; Losekoot M; Haak H; Heister GA; Giordano PC; Bernini LF
    Br J Haematol; 1994 May; 87(1):139-43. PubMed ID: 7947237
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Various α-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (α
    Al Moamen NJ; Thabet A; Mahdi F; Newton H; Salman E
    Hemoglobin; 2018 May; 42(3):166-170. PubMed ID: 30864492
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
    Adekile AD; Gu LH; Baysal E; Haider MZ; al-Fuzae L; Aboobacker KC; al-Rashied A; Huisman TH
    Acta Haematol; 1994; 92(4):176-81. PubMed ID: 7701914
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.
    Hellani A; Fadel E; El-Sadadi S; El-Sweilam H; El-Dawood A; Abu-Amero KK
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):219-21. PubMed ID: 19371220
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human beta-globin gene.
    Orkin SH; Cheng TC; Antonarakis SE; Kazazian HH
    EMBO J; 1985 Feb; 4(2):453-6. PubMed ID: 4018033
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An alpha-globin gene initiation codon mutation in a black family with HbH disease.
    Olivieri NF; Chang LS; Poon AO; Michelson AM; Orkin SH
    Blood; 1987 Sep; 70(3):729-32. PubMed ID: 3620699
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
    Fei YJ; Oner R; Bözkurt G; Gu LH; Altay C; Gurgey A; Fattoum S; Baysal E; Huisman TH
    Acta Haematol; 1992; 88(2-3):82-5. PubMed ID: 1281602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Haplotypes of alpha-globin-gene in the Saudi population--the triplicated gene (alpha alpha alpha anti 3.7/).
    el-Hazmi MA
    Hum Hered; 1987; 37(5):314-8. PubMed ID: 2822569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and - -
    Zhang Q; Fan X; Xu M; Zhang Y; Xu H; Wen X; Zhou W
    Hemoglobin; 2017 May; 41(3):189-192. PubMed ID: 28950779
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemia.
    Traeger-Synodinos J; Metaxotou-Mavrommati A; Karagiorga M; Vrettou C; Papassotiriou I; Stamoulakatou A; Kanavakis E
    Hemoglobin; 1999 Nov; 23(4):325-37. PubMed ID: 10569721
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unusual molecular basis of Hb H disease in the Azores Islands, Portugal.
    Romão L; Olim G; Martins MC; Rodrigues V; Coutinho-Gomes MP; Lavinha J
    Hemoglobin; 1990; 14(6):607-16. PubMed ID: 2101837
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).
    Liebhaber SA; Coleman MB; Adams JG; Cash FE; Steinberg MH
    J Clin Invest; 1987 Jul; 80(1):154-9. PubMed ID: 3597771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. α-Thalassemia syndromes in the United Arab Emirates.
    Baysal E
    Hemoglobin; 2011; 35(5-6):574-80. PubMed ID: 22074123
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alpha-thalassaemia caused by a polyadenylation signal mutation.
    Higgs DR; Goodbourn SE; Lamb J; Clegg JB; Weatherall DJ; Proudfoot NJ
    Nature; 1983 Nov 24-30; 306(5941):398-400. PubMed ID: 6646217
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia.
    Fortina P; Parrella T; Sartore M; Gottardi E; Gabutti V; Delgrosso K; Mansfield E; Rappaport E; Schwartz E; Camaschella C
    Blood; 1994 Jun; 83(11):3356-62. PubMed ID: 8193372
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new genetic basis for hemoglobin-H disease.
    Pressley L; Higgs DR; Clegg JB; Perrine RP; Pembrey ME; Weatherall DJ
    N Engl J Med; 1980 Dec; 303(24):1383-8. PubMed ID: 6253786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.