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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

197 related items for PubMed ID: 1163493

  • 21. Prevalence of alpha-chain variants at birth.
    Castro O, Winter WP, Lee TC, Headings VE.
    Am J Clin Pathol; 1981 Jan; 75(1):56-9. PubMed ID: 7457429
    [Abstract] [Full Text] [Related]

  • 22. A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.
    Di Iorio EE, Winterhalter KH, Wilson K, Rosenmund A, Marti HR.
    Blut; 1975 Aug; 31(2):61-8. PubMed ID: 1164567
    [Abstract] [Full Text] [Related]

  • 23. [Erythrocyte hypocromia in heterozygous hemoglobin E (beta 26 Glu replaced by Lys)].
    Keller P, Kohne E.
    Acta Haematol; 1976 Aug; 56(5):276-84. PubMed ID: 826084
    [Abstract] [Full Text] [Related]

  • 24. [A variant of abnormal hemoglobin D].
    Efremov G, Duma H, Sadikario A, Andreeva M, Mladenovski B, Petkov G.
    Acta Med Iugosl; 1967 Aug; 21(2):173-81. PubMed ID: 5189416
    [No Abstract] [Full Text] [Related]

  • 25. Hemoglobin Hijiyama: a new fast-moving hemoglobin in a Japanese family.
    Miyaji T, Oba Y, Yamamoto K, Shibata S, Iuchi I, Hamilton HB.
    Science; 1968 Jan 12; 159(3811):204-6. PubMed ID: 5634912
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Hb Hope [β136Gly→Asp] and Hb Grady [α119_120insGluPheThr] compound heterozygosity in a Mauritanian patient.
    Delacour H, Konopacki J, Plantamura J, Lacan P, Joly P.
    Clin Chem Lab Med; 2016 Feb 12; 54(2):e35-6. PubMed ID: 26351951
    [No Abstract] [Full Text] [Related]

  • 32. Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.
    Milner PF, Clegg JB, Weatherall DJ.
    Lancet; 1971 Apr 10; 1(7702):729-32. PubMed ID: 4101431
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS.
    Lutcher CL, Wilson JB, Gravely ME, Stevens PD, Chen CJ, Lindeman JG, Wong SC, Miller A, Gottleib M, Huisman TH.
    Blood; 1976 Jan 10; 47(1):99-112. PubMed ID: 1244915
    [Abstract] [Full Text] [Related]

  • 35. Genetic heterogeneity of thalassemias in Mexican mestizo patients with hemolytic anemia.
    Ibarra B, Vaca G, de la Mora E, Romero F, Aguilar-Luna C, Mejía A, Esparza MA, Pérez G, Ornelas ML, Cantú JM.
    Hum Hered; 1988 Jan 10; 38(2):95-100. PubMed ID: 2454217
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. [Hemoglobin G Coushatta (beta 22 (B4) glu leads to ala) in Algeria: an homozygous case].
    Boissel JP, Wajcman H, Labie D, Dahmane M, Benabadji M.
    Nouv Rev Fr Hematol (1978); 1979 Jan 10; 21(3):225-30. PubMed ID: 545312
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.