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Journal Abstract Search

121 related items for PubMed ID: 27117572

  • 21. Diagnosis and characterization of Hb C/Hb Iowa: a rare but easily misidentified compound heterozygous condition.
    Somjee S, Yu LC, Hagar AF, Hempe JM.
    Hemoglobin; 2004 Feb; 28(1):7-13. PubMed ID: 15008260
    [Abstract] [Full Text] [Related]

  • 22. Compound heterozygosity for hemoglobin C and hemoglobin Korle-Bu.
    Kossover CL, Eckman JR, Young AN.
    Lab Hematol; 2008 Feb; 14(3):30-4. PubMed ID: 18812284
    [Abstract] [Full Text] [Related]

  • 23. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
    Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.
    Hemoglobin; 2016 Feb; 40(1):64-5. PubMed ID: 26372199
    [Abstract] [Full Text] [Related]

  • 24. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012 Feb; 36(1):18-24. PubMed ID: 22145566
    [Abstract] [Full Text] [Related]

  • 25. Blood typing profile of a school-aged population of a North Togo township.
    Vovor A, Fétéké L, Kueviakoe IM, Kpatarou L, Mawussi K, Magnang H, Ségbéna AY.
    Hemoglobin; 2014 Feb; 38(5):316-8. PubMed ID: 25271992
    [Abstract] [Full Text] [Related]

  • 26. Clinical Course of Homozygous Hemoglobin Constant Spring in Pediatric Patients.
    Komvilaisak P, Jetsrisuparb A, Fucharoen G, Komwilaisak R, Jirapradittha J, Kiatchoosakun P.
    J Pediatr Hematol Oncol; 2018 Jul; 40(5):409-412. PubMed ID: 29668548
    [Abstract] [Full Text] [Related]

  • 27. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY, Yan JM, Li J, Li DZ.
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
    [Abstract] [Full Text] [Related]

  • 28. An infant with homozygous hemoglobin D-Iran.
    Thornburg CD, Zimmerman SA, Schultz WH, Ware RE.
    J Pediatr Hematol Oncol; 2001 Jan; 23(1):67-8. PubMed ID: 11196276
    [Abstract] [Full Text] [Related]

  • 29. An intriguing high performance liquid chromatogram of a double heterozygosity for Hb Q-India/Hb D-Punjab.
    Badyal RK, Chhabra S, Sharma P, Das R.
    Hemoglobin; 2014 Jan; 38(6):440-3. PubMed ID: 25354131
    [Abstract] [Full Text] [Related]

  • 30. Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.
    Parab S, Sakhare S, Sengupta C, Velumani A.
    Clin Chim Acta; 2015 Mar 10; 442():33-5. PubMed ID: 25576799
    [Abstract] [Full Text] [Related]

  • 31. Haplotype analysis of two new, independent cases of Hb Osu-Christiansborg.
    Giordano PC, Harteveld CL, Bernini LF, Doorduijn JK, Geenen AA, Kok PJ, Versteegh FG.
    Hemoglobin; 1999 May 10; 23(2):193-5. PubMed ID: 10335988
    [No Abstract] [Full Text] [Related]

  • 32. HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations.
    Haynes CA, Guerra SL, Fontana JC, DeJesús VR.
    Clin Chim Acta; 2013 Sep 23; 424():191-200. PubMed ID: 23796846
    [Abstract] [Full Text] [Related]

  • 33. Diagnostic Dilemma of Hb Perth [β32(B14)Leu→Pro; HBB: c.98T > C] in Mainland China.
    Jiang H, Yan JM, Li J, Xie XM, Li DZ.
    Hemoglobin; 2016 Jun 23; 40(3):202-5. PubMed ID: 27117570
    [Abstract] [Full Text] [Related]

  • 34. Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.
    Ferreira C, Hoyer JD, Miranda A, Picanço I, Almendra V, Seixas MT, Almeida T, Romão L, Faustino P.
    Am J Hematol; 2006 Apr 23; 81(4):256-61. PubMed ID: 16550507
    [Abstract] [Full Text] [Related]

  • 35. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov 23; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 36. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 Nov 23; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 37. A case of compound heterozygosity for Hb S and Hb S Oman.
    Al Jahdhamy R, Makki H, Farrell G, Al Azzawi S.
    Br J Haematol; 2002 Mar 23; 116(3):504. PubMed ID: 11849204
    [No Abstract] [Full Text] [Related]

  • 38. [Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family].
    Sousa Uva L, Fernandes A, Pilar M.
    Nouv Rev Fr Hematol (1978); 1983 Mar 23; 25(6):387-90. PubMed ID: 6664837
    [Abstract] [Full Text] [Related]

  • 39. Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A].
    Kutlar F, Unguru Y, Dixon N, Patel N, Bailey L, Zhuang L, Carmichael H, Kutlar A.
    Hemoglobin; 2014 Mar 23; 38(3):207-10. PubMed ID: 24471829
    [Abstract] [Full Text] [Related]

  • 40. Molecular diagnosis of a case of Hb Phnom Penh [alpha117(GH5)Phe-I1e-alpha118(H1)Thr (alpha1)].
    Leung RY, Ma ES, Chan AY, Chow EY.
    Hemoglobin; 2006 Mar 23; 30(3):397-9. PubMed ID: 16840232
    [Abstract] [Full Text] [Related]

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