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 *

202 related articles for article (PubMed ID: 2995233)

  • 1. Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families.
    Griese EU; Kohne E; Horst J
    Hum Genet; 1985; 71(2):134-7. PubMed ID: 2995233
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
    Nicholls RD; Higgs DR; Clegg JB; Weatherall DJ
    Blood; 1985 Jun; 65(6):1434-8. PubMed ID: 2986746
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
    Pressley L; Higgs DR; Clegg JB; Weatherall DJ
    Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3586-9. PubMed ID: 6158051
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alpha zero- and beta zero-thalassemia in a Thai family: unusually mild homozygous beta zero-thalassemia without alpha-globin gene deletion.
    Yenchitsomanus P; Summers KM
    Hum Genet; 1985; 69(4):375-7. PubMed ID: 2580774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterisation of a new alpha thalassemia 1 defect due to a partial deletion of the alpha globin gene complex.
    Pressley L; Higgs DR; Aldridge B; Metaxatou-Mavromati A; Clegg JB; Weatherall DJ
    Nucleic Acids Res; 1980 Nov; 8(21):4889-98. PubMed ID: 6255436
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
    Galanello R; Melis MA; Maccioni L; Pirastu M; Cao A
    Pediatr Res; 1984 Feb; 18(2):158-62. PubMed ID: 6322098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
    Embury SH; Miller JA; Dozy AM; Kan YW; Chan V; Todd D
    J Clin Invest; 1980 Dec; 66(6):1319-25. PubMed ID: 7440717
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency and types of deletional alpha+-thalassemia in northern Sardinia.
    Di Rienzo A; Felicetti L; Novelletto A; Forteleoni G; Colombo B
    Hum Genet; 1985; 71(2):147-9. PubMed ID: 2995236
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene.
    Kulozik AE; Kar BC; Serjeant GR; Serjeant BE; Weatherall DJ
    Blood; 1988 Feb; 71(2):467-72. PubMed ID: 2827816
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Specific abnormalities of globin gene organization in the thalassemia syndromes.
    Orkin SH
    Ann N Y Acad Sci; 1980; 344():48-61. PubMed ID: 6249172
    [No Abstract]   [Full Text] [Related]  

  • 17. Alpha-thalassemia in Saudi Arabia: deletion pattern.
    el-Hazmi MA
    Hum Genet; 1987 Jun; 76(2):196-8. PubMed ID: 3038731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dysfunctional alpha-globin genes in hemoglobin H disease in blacks: variation in restriction fragment size permits the detection of the -alpha/-alpha T genotype.
    Safaya S; Mullaney P; Rieder RF
    Am J Hematol; 1987 Dec; 26(4):329-39. PubMed ID: 2891296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Alpha-thalassemia screening reveals quadruple zeta-globin genes in a Laotian family.
    Titus EA; Hsia YE; Hunt JA
    Hemoglobin; 1988; 12(5-6):539-50. PubMed ID: 3209396
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.