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2. 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]
3. A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families. Sukumaran PK, Huisman TH, Schroeder WA, McCurdy PR, Freehafer JT, Bouver N, Shelton JR, Shelton JB, Apell G. Br J Haematol; 1972 Oct; 23(4):403-17. PubMed ID: 5084806 [No Abstract] [Full Text] [Related]
7. Is haemoglobin G Philadelphia linked to -thalassaemia? French EA, Lehmann H. Acta Haematol; 1971 Oct; 46(3):149-56. PubMed ID: 5001519 [No Abstract] [Full Text] [Related]
9. Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18). Sharma RS, Williams L, Wilson JB, Huisman TH. Biochim Biophys Acta; 1975 Jun 26; 393(2):379-82. PubMed ID: 1148221 [Abstract] [Full Text] [Related]
11. Haemoglobin LeporeBoston in a Turkish family. Cavdar AO, Arcasoy A. J Med Genet; 1976 Oct 26; 13(5):363-5. PubMed ID: 1003447 [Abstract] [Full Text] [Related]
12. [A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families]. Echavarria A, Molina C, Zapata CI. Sangre (Barc); 1973 Oct 26; 18(2):145-56. PubMed ID: 4753554 [No Abstract] [Full Text] [Related]