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 *

105 related articles for article (PubMed ID: 4023693)

  • 1. Triplicated alpha-globin gene loci in a Chinese family.
    Zhang JW; Wu GY; Yang XY; Yang TY
    Sci Sin B; 1985 Jun; 28(6):626-31. PubMed ID: 4023693
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interaction of chromosomes bearing 1, 2 or 3 alpha-globin genes in an American black family with alpha-thalassemia.
    Sancar GB; Cedeno MM; Bellevue R; Rieder RF
    Hemoglobin; 1982; 6(2):99-114. PubMed ID: 7096114
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High frequency of triplicated alpha-globin loci and absence or low frequency of alpha thalassemia in Polynesian Samoans.
    Lie-Injo LE; Pawson IG; Solai A
    Hum Genet; 1985; 70(2):116-8. PubMed ID: 2989152
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A family with segregating triplicated alpha globin loci and beta thalassemia.
    Galanello R; Ruggeri R; Paglietti E; Addis M; Melis MA; Cao A
    Blood; 1983 Nov; 62(5):1035-40. PubMed ID: 6313095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Interaction of heterozygous beta (0)-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family.
    Beris P; Darbellay R; Hochmann A; Pradervand E; Pugin P
    Klin Wochenschr; 1991 Oct; 69(15):710-4. PubMed ID: 1795494
    [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. 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]  

  • 9. 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]  

  • 10. Mapping the alpha-globin genes in an Algerian HbH patient and his family.
    Whitelaw E; Pagnier J; Verdier G; Henni T; Godet J; Williamson R
    Blood; 1980 Mar; 55(3):511-6. PubMed ID: 7357081
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular diagnosis of beta-thalassemia intermedia].
    Chen J; Liu W; Chen M
    Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
    Phillips JA; Vik TA; Scott AF; Young KE; Kazazian HH; Smith KD; Fairbanks VF; Koenig HM
    Blood; 1980 Jun; 55(6):1066-9. PubMed ID: 6246995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compensatory increase in alpha 1-globin gene expression in individuals heterozygous for the alpha-thalassemia-2 deletion.
    Liebhaber SA; Cash FE; Main DM
    J Clin Invest; 1985 Sep; 76(3):1057-64. PubMed ID: 4044827
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Anthropogenetical analysis of abnormal human alpha-globin gene cluster arrangement on chromosome 16.
    Turcinov D; Krishnamoorthy R; Janićijević B; Marković I; Mustać M; Lapoumeroulie C; Chaventré A; Rudan P
    Coll Antropol; 2000 Dec; 24(2):295-301. PubMed ID: 11216396
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. A novel alpha-globin gene arrangement in man.
    Higgs DR; Old JM; Pressley L; Clegg JB; Weatherall DJ
    Nature; 1980 Apr; 284(5757):632-5. PubMed ID: 6245373
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype.
    Galanello R; Paglietti E; Melis MA; Giagu L; Cao A
    Acta Haematol; 1984; 72(1):34-6. PubMed ID: 6089487
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
    Lie-Injo LE; Dozy AM; Kan YW; Lopes M; Todd D
    Blood; 1979 Dec; 54(6):1407-16. PubMed ID: 508945
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.