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Journal Abstract Search

160 related items for PubMed ID: 15768554

  • 41.
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  • 42. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K, Sriphaisal T, Krutvecho T, Ketupanya A, Vuthiwong C, Suwanasophon C, Noonai A.
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():287-90. PubMed ID: 8629126
    [Abstract] [Full Text] [Related]

  • 43. Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.
    Harteveld CL, van Helden WC, Boxma GL, van Delft P, Bakker-Verweij M, Wajcman H, Zanella-Cleon I, Becchi M, Giordano PC.
    Hemoglobin; 2007; 31(3):325-32. PubMed ID: 17654069
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  • 48. Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method.
    Sura T, Trachoo O, Viprakasit V, Vathesatogkit P, Tunteeratum A, Busabaratana M, Wisedpanichkij R, Isarangkura P.
    Ann Hematol; 2007 Sep; 86(9):659-63. PubMed ID: 17503046
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  • 49. 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; 79(5):422-8. PubMed ID: 17916081
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  • 50. Spectrum of α-globin gene mutations in the Kerman Province of Iran.
    Saleh-Gohari N, Khosravi-Mashizi A.
    Hemoglobin; 2010 Nov; 34(5):451-60. PubMed ID: 20854119
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  • 51. 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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  • 52. Molecular basis of alpha-thalassemia in Algeria.
    Mesbah-Amroun H, Rouabhi F, Ducrocq R, Elion J.
    Hemoglobin; 2008 Sep; 32(3):273-8. PubMed ID: 18473243
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  • 53. Four cases of Hb Q-H disease found in Southern China.
    Li D, Liao C, Xie X, Zhong H, Li J.
    Hemoglobin; 2007 Sep; 31(1):109-11. PubMed ID: 17365013
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  • 54. Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA].
    Harteveld CL, Traeger-Synodinos J, Ragusa A, Fichera M, Kanavakis E, Kattamis C, Giordano P, Schilirò G, Bernini LF.
    Haematologica; 2001 Jan; 86(1):36-8. PubMed ID: 11146568
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  • 55. Phenotypic variability in a chinese family with nondeletional Hb H-Hb Quong Sze disease.
    Li J, Liao C, Zhou JY, Xie XM, Li R, Chen LH, Li DZ.
    Hemoglobin; 2011 Jan; 35(4):430-3. PubMed ID: 21797711
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  • 56. Molecular spectrum of alpha-thalassemia in the Iranian population of Hormozgan: three novel point mutation defects.
    Harteveld CL, Yavarian M, Zorai A, Quakkelaar ED, van Delft P, Giordano PC.
    Am J Hematol; 2003 Oct; 74(2):99-103. PubMed ID: 14508795
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  • 57. Alpha-thalassaemia and population health in Southeast Asia.
    Chui DH.
    Ann Hum Biol; 2005 Oct; 32(2):123-30. PubMed ID: 16096207
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  • 58. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG, Bhanushali AA, Dedhia P, Jeswani KD, Dayanand S, Dasgupta A, Das BR.
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
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  • 59.
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  • 60. Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.
    Chui DH.
    Ann N Y Acad Sci; 2005 Sep; 1054():25-32. PubMed ID: 16339648
    [Abstract] [Full Text] [Related]

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