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Journal Abstract Search

109 related items for PubMed ID: 3727027

  • 1.
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  • 2. Clinical and hematological features of homozygous hemoglobin O-Arab [beta 121 Glu → Lys].
    Dror S.
    Pediatr Blood Cancer; 2013 Mar; 60(3):506-7. PubMed ID: 23192960
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  • 3. [Hemoglobin O Arab--beta-thalassemia in a Bulgarian, a resident of Odessa].
    Adamovskaia II, Idel'son LI, Matragun S, Lehmann H.
    Probl Gematol Pereliv Krovi; 1978 Mar; 23(11):51-3. PubMed ID: 714895
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  • 4. Hemoglobin SO Arab and hemoglobin CO Arab diseases. Clinical and laboratory study.
    Maeda K, Kini RK, Saeed SM, Rucknagel DL.
    Am J Pediatr Hematol Oncol; 1983 Mar; 5(2):127-31. PubMed ID: 6614393
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  • 5. [Rare variants of Hb D Punjab, Hb O Arab and polymorphism of human hemoglobins].
    Spivak VA, Tasheva ES, Aseeva EA, Tokarev IuN.
    Genetika; 1986 Mar; 22(3):511-8. PubMed ID: 3957034
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  • 11. Clinical phenotypes and genotypes diagnosis of thalassemia in children.
    Torcharus K, Sriphaisal T, Krutvecho T, Suwanasophon C, Intarapakawong J.
    Southeast Asian J Trop Med Public Health; 1995 Mar; 26 Suppl 1():275-7. PubMed ID: 8629123
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  • 12. [Hemoglobin O Arab in Ivory Coast and western Africa].
    Sangare A, Sanogo I, Meite M, Ambofo Y, Abesopie V, Segbena A, Tolo A.
    Med Trop (Mars); 1992 Mar; 52(2):163-7. PubMed ID: 1328806
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  • 13. [Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies].
    Indrák K, Divoký V, Kynclová E, Divoká M, Melichárková R, Indráková J.
    Vnitr Lek; 1998 Jun; 44(6):347-9. PubMed ID: 9820058
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  • 15. Allele related mutation specific-polymerase chain reaction for rapid diagnosis of Hb New York (beta 113 (G15) Val-->Glu, beta(CD113 GTG-->GAG)).
    Viprakasit V, Tachavanich K, Suwantol L, Pung-Amritt P, Chinchang W, Tanphaichitr VS.
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S558-63. PubMed ID: 12403232
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  • 16. Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
    Sura T, Busabaratana M, Youngcharoen S, Wisedpanichkij R, Viprakasit V, Trachoo O.
    Eur J Haematol; 2007 Sep; 79(3):251-4. PubMed ID: 17655700
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  • 17. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha16(A14)Lys-->Asn] and Hb E [beta26(B8)Glu-->Lys] with a deletional alpha-thalassemia-1 in a Thai family.
    Fucharoen S, Chunpanich S, Sanchaisuriya K, Fucharoen G, Kunyanone N.
    Hemoglobin; 2005 Sep; 29(1):77-83. PubMed ID: 15768559
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  • 18. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients.
    Fucharoen S, Singsanan S, Sanchaisuriya K, Fucharoen G.
    Clin Lab Haematol; 2005 Jun; 27(3):184-9. PubMed ID: 15938724
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  • 19. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.
    Southeast Asian J Trop Med Public Health; 1995 Jun; 26 Suppl 1():252-6. PubMed ID: 8629117
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  • 20. [Association of hemoglobin E and thalassemia].
    Schaison G, Leverger G, Vidaud M.
    Arch Fr Pediatr; 1985 Oct; 42(8):709-11. PubMed ID: 4074101
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