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 *

143 related articles for article (PubMed ID: 1787106)

  • 1. Hb Strumica [alpha(2)112(G19)His----Arg beta 2] in a Turkish family.
    Akar N; Arcasoy A; Ata Y
    Hemoglobin; 1991; 15(4):347-8. PubMed ID: 1787106
    [No Abstract]   [Full Text] [Related]  

  • 2. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].
    Adams JG; Steinberg MH; Newman MV; Morrison WT; Benz EJ; Iyer R
    Proc Natl Acad Sci U S A; 1981 Jan; 78(1):469-73. PubMed ID: 6165992
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect.
    Turbpaiboon C; Svasti S; Sawangareetakul P; Winichagoon P; Srisomsap C; Siritanaratkul N; Fucharoen S; Wilairat P; Svasti J
    Hemoglobin; 2002 Feb; 26(1):77-81. PubMed ID: 11939517
    [No 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. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F; Chadli A; Fattoum S; Souilem J; Hassine L
    Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.
    Felice AE; Ozdonmez R; Headlee ME; Huisman TH
    Biochem Genet; 1982 Aug; 20(7-8):689-701. PubMed ID: 6291506
    [No Abstract]   [Full Text] [Related]  

  • 7. Association of beta-thalassemia and Hb Q-Thailand resulting in a normal Hb A2 value.
    Liao C; Li J; Li D
    Hemoglobin; 2008; 32(5):505-8. PubMed ID: 18932077
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family.
    Gu YC; Gu LH; Wilson JB; Cepreganova B; Ramachandran M; Walker EL; Huisman TH; Potitong P
    Hemoglobin; 1991; 15(4):297-302. PubMed ID: 1787098
    [No Abstract]   [Full Text] [Related]  

  • 9. Hb N-Baltimore [alpha 2 beta 2(95)(FG2)Lys----Glu] and Hb J-Iran [alpha 2 beta 2(77)(Ef1]His----Asp] observed in a Turkish family from Antalya.
    Bircan I; Güven AG; Yegin O; Plaseska D; Wilson JB; Ramachandran M; Huisman TH
    Hemoglobin; 1990; 14(4):453-7. PubMed ID: 2283300
    [No Abstract]   [Full Text] [Related]  

  • 10. A second observation of Hb Abruzzo [alpha 2 beta 2(143)(H21)His----Arg] in an Italian family.
    Zhao W; Wilson JB; Webber BB; Huisman TH; Sciarratta GV; Ivaldi G; Ripamonti M
    Hemoglobin; 1990; 14(4):463-6. PubMed ID: 2283302
    [No Abstract]   [Full Text] [Related]  

  • 11. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL; Steen G; Vlasveld LT; van Delft P; Giordano PC
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Hb J Cape Town homozygote--association of Hb J Cape Town and alpha-thalassaemia.
    Botha MC; Stathopoulou R; Lehmann H; Rees JS; Plowman D
    FEBS Lett; 1978 Dec; 96(2):331-4. PubMed ID: 729801
    [No Abstract]   [Full Text] [Related]  

  • 13. The haematological puzzle of Hb J Cape Town is partly solved.
    Lambridis AJ; Ramsay M; Jenkins T
    Br J Haematol; 1986 Jun; 63(2):363-7. PubMed ID: 3718876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb Prato [alpha31(B12)Arg --> Ser (A2)] and alpha-thalassemia in a Taiwanese.
    Shih MC; Peng CT; Chang JY; Liu SC; Kuo PL; Chang JG
    Hemoglobin; 2003 Feb; 27(1):45-7. PubMed ID: 12603094
    [No Abstract]   [Full Text] [Related]  

  • 15. Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
    Gurgey A; Altay C; Beksaç MS; Bhattacharya R; Kutlar F; Huisman TH
    Acta Haematol; 1989; 81(3):169-71. PubMed ID: 2496567
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Beta-thalassemia in Yugoslavia.
    Dimovski A; Efremov DG; Jankovic L; Juricic D; Zisovski N; Stojanovski N; Nikolov N; Petkov GT; Reese AL; Stoming TA
    Hemoglobin; 1990; 14(1):15-24. PubMed ID: 2200761
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mapping the alpha-globin genes in Hb J Mexico carriers.
    Trabuchet G; Morle F; Verdier G; Godet J; Benabadji M; Nigon VM
    Hum Genet; 1982; 62(2):164-6. PubMed ID: 6298095
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Developmental effect of the XmnI site on Ggamma-globin gene expression among newborn Hb F-Malta-I [Ggamma117(G19)His-->Arg, CAT-->CGT] heterozygotes and adult beta+ -Thalassemia homozygotes.
    Pulis S; Scerri CA; Wismayer PS; Galdies R; Wettinger SB; Felice AE
    Hemoglobin; 2007; 31(1):71-82. PubMed ID: 17365007
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Silent beta-thalassemia and thalassemia intermedia.
    Huisman TH
    Haematologica; 1990; 75 Suppl 5():1-8. PubMed ID: 2086369
    [No Abstract]   [Full Text] [Related]  

  • 20. Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family.
    Malcorra-Azpiazu JJ; Balda-Aguirre MI; Diaz-Chico JC; Kutlar F; Kutlar A; Wilson JB; Hu H; Huisman TH
    Hemoglobin; 1988; 12(2):201-5. PubMed ID: 3384713
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.