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Journal Abstract Search
125 related items for PubMed ID: 893136
1. Homozygous hemoglobin O Arab in a gypsy family in Yugoslavia. Efremov GD, Sadikario A, Stojancov A, Dojcinov D, Huisman TH. Hemoglobin; 1977; 1(4):389-94. PubMed ID: 893136 [No Abstract] [Full Text] [Related]
8. Abnormal hemoglobins in the Takamatsu district with emphasis on epidemiological characteristics. Iuchi I, Hidaka K, Shimasaki S, Shibata S, Ueda S, Mizushima M, Aoba H. Hemoglobin; 1982 Jan; 6(5):493-502. PubMed ID: 7174348 [No Abstract] [Full Text] [Related]
12. [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; 21(3):225-30. PubMed ID: 545312 [Abstract] [Full Text] [Related]
13. Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity. Beutler E, Lang A, Lehmann H. Blood; 1974 Apr; 43(4):527-35. PubMed ID: 4361395 [No Abstract] [Full Text] [Related]
14. Various aspects of alpha-thalassemia. Lehmann H, Lang A. Ann N Y Acad Sci; 1974 Apr; 232(0):152-8. PubMed ID: 4370548 [No Abstract] [Full Text] [Related]
15. A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia. Weatherall DJ, Clegg JB, Blankson J, McNeil JR. Br J Haematol; 1969 Dec; 17(6):517-26. PubMed ID: 5357741 [No Abstract] [Full Text] [Related]