BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

371 related articles for article (PubMed ID: 2983536)

  • 1. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE; Herrera AR; Lebo RV; Hassan K; Lopez CG
    Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hb Bart's level in cord blood and deletions of alpha-globin genes.
    Lie-Injo LE; Solai A; Herrera AR; Nicolaisen L; Kan YW; Wan WP; Hasan K
    Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.
    Orkin SH; Old J; Lazarus H; Altay C; Gurgey A; Weatherall DJ; Nathan DG
    Cell; 1979 May; 17(1):33-42. PubMed ID: 455460
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of Hb Bart's Hydrops Fetalis Caused by - -
    He S; Li J; Huang P; Zhang S; Lin L; Zuo Y; Tian X; Zheng C; Qiu X; Chen B
    Hemoglobin; 2018 Jan; 42(1):61-64. PubMed ID: 29493331
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The levels of zeta, gamma, and delta chains in patients with Hb H disease.
    Kutlar F; Gonzalez-Redondo JM; Kutlar A; Gurgey A; Altay C; Efremov GD; Kleman K; Huisman TH
    Hum Genet; 1989 May; 82(2):179-86. PubMed ID: 2566576
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
    Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hydrops fetalis due to an unusual form of Hb H disease.
    Chan V; Chan TK; Liang ST; Ghosh A; Kan YW; Todd D
    Blood; 1985 Jul; 66(1):224-8. PubMed ID: 2988669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular basis of alpha-thalassaemia in Thailand.
    Winichagoon P; Higgs DR; Goodbourn SE; Clegg JB; Weatherall DJ; Wasi P
    EMBO J; 1984 Aug; 3(8):1813-8. PubMed ID: 6548185
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
    Wang W; Yap CH; Loh SF; Tan AS; Lim MN; Prasath EB; Chan ML; Tan WC; Jiang B; Yeo GH; Mathew J; Ho A; Ho SS; Wong PC; Choolani MA; Chong SS
    Reprod Biomed Online; 2010 Nov; 21(5):642-8. PubMed ID: 20864413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of zeta-globin chains in the cord blood by ELISA (enzyme-linked immunosorbent assay): rapid screening for alpha-thalassemia 1 (Southeast Asian type).
    Ausavarungnirun R; Winichagoon P; Fucharoen S; Epstein N; Simkins R
    Am J Hematol; 1998 Apr; 57(4):283-6. PubMed ID: 9544971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia.
    King AJ; Higgs DR
    Hematology Am Soc Hematol Educ Program; 2018 Nov; 2018(1):353-360. PubMed ID: 30504332
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
    Steinberg MH; Coleman MB; Adams JG; Hartmann RC; Saba H; Anagnou NP
    Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Genetic and molecular diversity in nondeletion Hb H disease.
    Higgs DR; Pressley L; Aldridge B; Clegg JB; Weatherall DJ; Cao A; Hadjiminas MG; Kattamis C; Metaxatou-Mavromati A; Rachmilewitz EA; Sophocleous T
    Proc Natl Acad Sci U S A; 1981 Sep; 78(9):5833-7. PubMed ID: 6272319
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The relationship between Hb Bart's levels in cord blood and the deletions of alpha-globin genes.
    Zhao W; Zhang J; Wang NS; Deng P
    Hemoglobin; 1988; 12(5-6):519-27. PubMed ID: 3209394
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of Chinese homozygous alpha-thalassaemia 1 and haemoglobin H disease by analysis of alpha- and phi zeta-globin genes in chorionic villi and amniocytes.
    Ko TM; Hsieh FJ; Hsu PM; Lee TY
    Prenat Diagn; 1989 Oct; 9(10):715-25. PubMed ID: 2594699
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 19.