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 *

80 related articles for article (PubMed ID: 6166591)

  • 1. The first homozygote for the hereditary persistence of fetal hemoglobin observed in the southeastern United States.
    Huisman TH
    Hemoglobin; 1981; 5(4):411-6. PubMed ID: 6166591
    [No Abstract]   [Full Text] [Related]  

  • 2. Homozygotes for the hereditary persistence of fetal hemoglobin: the ratio of G gamma to A gamma chains and biosynthetic studies.
    Ringelhann B; Acquaye CT; Oldham JH; Konotey-Ahulu FI; Yawson G; Sukumaran PK; Schroeder WA; Huisman TH
    Biochem Genet; 1977 Dec; 15(11-12):1083-96. PubMed ID: 603615
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new type of hereditary persistence of fetal haemoglobin (HPFH): HPFH Tunisia beta + (+C-200)G gamma.
    Pissard S; M'rad A; Beuzard Y; Roméo PH
    Br J Haematol; 1996 Oct; 95(1):67-72. PubMed ID: 8857940
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The polymorphism of human fetal hemoglobin.
    Huisman TH
    Birth Defects Orig Artic Ser; 1982; 18(7):83-99. PubMed ID: 6186316
    [No Abstract]   [Full Text] [Related]  

  • 5. Homozygous hemoglobin D Punjab.
    Ozsoylu S
    Acta Haematol; 1970; 43(6):353-9. PubMed ID: 4991321
    [No Abstract]   [Full Text] [Related]  

  • 6. Blood-donor homozygous for hereditary persistence of fetal haemoglobin.
    Acquaye CT; Oldham JH; Konotey-Ahulu FI
    Lancet; 1977 Apr; 1(8015):796-7. PubMed ID: 66588
    [No Abstract]   [Full Text] [Related]  

  • 7. Hb A2-Babinga, Hb S, and HPFH in members of a family from Creola, Alabama.
    McRoyan DK; Liu PI; Mankad VN; Wilson JB; Huisman TH
    Hemoglobin; 1984; 8(4):413-6. PubMed ID: 6207140
    [No Abstract]   [Full Text] [Related]  

  • 8. Another form of the hereditary persistence of fetal hemoglobin (the Atlanta type)?
    Altay C; Huisman TH; Schroeder WA
    Hemoglobin; 1976-1977; 1(2):125-33. PubMed ID: 1052176
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin.
    Old JM; Ayyub H; Wood WG; Clegg JB; Weatherall DJ
    Science; 1982 Feb; 215(4535):981-2. PubMed ID: 6186021
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The gamma-chain in a Ghanaian adult, homozygous for hereditary persistence of fetal haemoglobin.
    Kamuzora H; Ringelhann B; Konotey-Ahulu FI; Lehmann H; Lorkin PA
    Acta Haematol; 1974; 51(3):179-84. PubMed ID: 4218432
    [No Abstract]   [Full Text] [Related]  

  • 11. Analysis of the gamma chains in a homozygote for HPFH Negro type and in three related heterozygotes.
    Guerrasio A; Acquaye CT; Oldham JH; Sartoris ML; Camaschella C; Saglio G; Mazza U
    Acta Haematol; 1980; 63(3):146-50. PubMed ID: 6155042
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A mutation associated with elevated G gamma chain in sickle cell anemia and hereditary persistence of fetal hemoglobin.
    Gilman JG; Huisman TH
    Prog Clin Biol Res; 1985; 191():141-9. PubMed ID: 2413470
    [No Abstract]   [Full Text] [Related]  

  • 13. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Grisanti P; Ponzini D; Di Biagio P
    Int J Lab Hematol; 2014 Feb; 36(1):13-9. PubMed ID: 23621512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia.
    Hattori Y; Kutlar F; Kutlar A; McKie VC; Huisman TH
    Hemoglobin; 1986; 10(6):623-42. PubMed ID: 2435679
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Ghanaian adult, homozygous for hereditary persistence of foetal haemoglobin and heterozygous for elliptocytosis.
    Ringelhann B; Konotey-Ahulu FI; Lehmann H; Lorkin PA
    Acta Haematol; 1970; 43(2):100-10. PubMed ID: 4986189
    [No Abstract]   [Full Text] [Related]  

  • 16. Sequence variations in the 3' A gamma enhancer are silent polymorphisms.
    Ragusa A; Lombardo M; Lombardo T; Beldjord C; Nagel RL; Elion J; Labie D; Krishnamoorthy R
    Prog Clin Biol Res; 1989; 316B():409-17. PubMed ID: 2482506
    [No Abstract]   [Full Text] [Related]  

  • 17. Indirect antiglobulin test and anti-D prophylaxis in hereditary persistence of fetal hemoglobin.
    Fadel HE; Krauss JS
    Obstet Gynecol; 1986 Mar; 67(3 Suppl):13S-14S. PubMed ID: 2418396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and molecular analysis of mild forms of homozygous beta-thalassemia.
    Weatherall DJ; Wainscoat JS; Thein SL; Old JM; Wood WG; Higgs DR; Clegg JB
    Ann N Y Acad Sci; 1985; 445():68-80. PubMed ID: 2409878
    [No Abstract]   [Full Text] [Related]  

  • 19. Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH.
    Braghini CA; Costa FC; Fedosyuk H; Neades RY; Novikova LV; Parker MP; Winefield RD; Peterson KR
    Exp Biol Med (Maywood); 2016 Apr; 241(7):697-705. PubMed ID: 26946532
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frequency of hemoglobin E/β-thalassemia compound heterozygotes with low hemoglobin F phenotype among cases with a diagnosis of hemoglobin E homozygote, determined by high-performance liquid chromatography, in prenatal control program for β-thalassemia.
    Wong P; Srichaiya A; Suannum P; Charoenporn P; Jermnim S; Chan-In M; Tapprom A; Deoisares R
    Ann Hematol; 2017 Oct; 96(10):1763-1765. PubMed ID: 28803407
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.