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 *

106 related articles for article (PubMed ID: 2318293)

  • 1. 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]  

  • 2. [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]  

  • 3. Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
    Embury SH; Lebo RV; Dozy AM; Kan YW
    J Clin Invest; 1979 Jun; 63(6):1307-10. PubMed ID: 447845
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Clinical severity of non-deletion form of HbH disease (--Med/alpha alpha thal).
    Di Marzo R; Lo Gioco P; Giambona A; Acuto S; Sammarco P; Oddo G; Maggio A
    Scand J Haematol; 1986 Jan; 36(1):39-43. PubMed ID: 3006223
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Molecular nature of deletion in beta 0-thalassemia, established using a method of amplification of genomic DNA in vitro].
    Shvarts EI; Gol'tsov AA; Kaboev OK; Bakhlanova IN; Alekseev AN
    Bioorg Khim; 1989 Apr; 15(4):556-9. PubMed ID: 2546567
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
    Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
    Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Characterization of a new alpha-thalassemia-1 deletion in a Spanish family.
    Gonzalez-Redondo JM; Gilsanz F; Ricard P
    Hemoglobin; 1989; 13(2):103-16. PubMed ID: 2544542
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R; Podda A; Melis MA; Monne M; Cao A
    Prog Clin Biol Res; 1989; 316B():113-21. PubMed ID: 2482492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A study of alpha thalassaemia families in western Saudi Arabia.
    Acquaye J; Ganeshaguru K; Sejeny S; Selchouk S; Hassounah F; Samuel A; Omer A
    Trop Geogr Med; 1985 Dec; 37(4):319-27. PubMed ID: 4095770
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alpha thalassaemia in the Maori: a family study.
    Parker LS; Williamson D; Shepherd CS; Boswell DR
    N Z Med J; 1989 May; 102(868):245-6. PubMed ID: 2471123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.
    Horst J; Griese EU; Kleihauer E; Kohne E
    Hum Genet; 1984; 68(3):260-3. PubMed ID: 6094337
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene.
    Motum PI; Lindeman R; Hamilton TJ; Trent RJ
    Br J Haematol; 1992 Sep; 82(1):107-13. PubMed ID: 1419783
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Partial deletion of the beta-globin gene: a common beta-thalassaemia allele in Asian Indians.
    Wood S; Daya M; Allanson JE; Kirby L; Coupland R; Gray GR
    Can J Genet Cytol; 1984 Jun; 26(3):296-301. PubMed ID: 6329492
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alpha globin gene analysis in a Sardinian family with interacting alpha and beta thalassaemia genes.
    Melis MA; Galanello R; Cao A
    Br J Haematol; 1983 Apr; 53(4):667-71. PubMed ID: 6299325
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.