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Journal Abstract Search

229 related items for PubMed ID: 741340

  • 1. [Concurrence on two siblings of three haemoglobin abnormal genes: haemoglobin S, beta-thalassaemia and hereditary persistence of foetal haemoglobin (author's transl)].
    Guerrero García R, Rosillo de León J, Landero de Ruíz N, Padilla C, Ruíz Reyes G.
    Sangre (Barc); 1978; 23(5):578-86. PubMed ID: 741340
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  • 3. [Genetic and hematological study of a family from Ghana suffering from hereditary persistence of fetal hemoglobin associated with beta-thalassemia and hemoglobinosis S].
    Boreux G, Wyss M, Farquet JJ.
    Arch Genet (Zur); 1973; 46(1):22-33. PubMed ID: 4731929
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  • 6. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F, Chadli A, Fattoum S, Souilem J, Hassine L.
    Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
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  • 7. [Haemoglobinosis C/beta-thalassemia double heterozygosity in an Algerian patient with total suppression of haemoglobin A synthesis (author's transl)].
    Boreux G, Farquet JJ, Pugin P, Miescher PA, Klein D.
    J Genet Hum; 1978 Mar; 26(1):1-15. PubMed ID: 670935
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  • 9. [Cooley's anemia syndrome in a double heterozygote for hemoglobin Lepore Washington-Boston and beta thalassemia].
    Ortega JJ, Baiget M, Aulesa C, Alonso JL.
    Med Clin (Barc); 1984 Nov 24; 83(17):717-20. PubMed ID: 6084156
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  • 13. 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 Nov 24; 38(2):95-100. PubMed ID: 2454217
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  • 17. [Studies on abnormal hemoglobins in China. 1. The structural analysis of a case of hemoglobin E in combination with thalassemia (author's transl)].
    Liang CC, Chen SS, Jia BC, Wang LF, Chen XY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1980 Mar 24; 2(1):9-16. PubMed ID: 6449309
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  • 18. [Heterozygous beta-thalassemia without icrease of hemoglobin A2].
    Marti HR, Grieder HR.
    Schweiz Med Wochenschr; 1970 Apr 11; 100(15):663-6. PubMed ID: 5438669
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  • 20. [A Japanese family with hereditary HbH disease--a case report and its gene analysis].
    Hattori Y, Yamashiro Y, Yamamoto K, Morishita M, Miyaji T, Yamamoto K, Matsuno Y, Fujii H, Miwa S, Ichimaru M.
    Rinsho Ketsueki; 1990 Feb 11; 31(2):183-8. PubMed ID: 2329681
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