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3. Haemoglobin synthesis in thalassaemia: two new molecular mechanisms for the production of the clinical picture of thalassaemia. Weatherall DJ; Clegg JB Hamatol Bluttransfus; 1972; 10():237-9. PubMed ID: 4667994 [No Abstract] [Full Text] [Related]
4. alpha-Thalassaemia in Sardinian infants. Galanello R; Diana G; Furbetta M; Angius A; Melis MA; Rosatelli C; Cao A J Med Genet; 1980 Oct; 17(5):357-62. PubMed ID: 7218276 [TBL] [Abstract][Full Text] [Related]
5. Haemoglobin Lepore Boston-Washington in Sicily: clinical, haematological, and biosynthetic studies. Schiliro G; Musumeci S; Pizzarelli G; Fischer A; Romero MA; Russo G J Med Genet; 1980 Jun; 17(3):179-82. PubMed ID: 7401128 [TBL] [Abstract][Full Text] [Related]
6. The alpha-chain-termination mutants and their relation to the alpha-thalassaemias. Weatherall DJ; Clegg JB Philos Trans R Soc Lond B Biol Sci; 1975 Aug; 271(913):411-55. PubMed ID: 240178 [TBL] [Abstract][Full Text] [Related]
7. Alpha-thalassaemia trait in various racial groups in the United Kingdom: characterization of a variant of alpha-thalassaemia in Indians. Walford DM; Deacon R Br J Haematol; 1976 Oct; 34(2):193-206. PubMed ID: 974033 [TBL] [Abstract][Full Text] [Related]
8. Haemoglobin D Los Angeles, D-beta +-thalassaemia, and D-beta o-thalassaemia. A report of two Canadian families. Wong SC; Ali MA Acta Haematol; 1980; 63(3):151-5. PubMed ID: 6769280 [TBL] [Abstract][Full Text] [Related]
10. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots. Jindatanmanusan P; Riolueang S; Glomglao W; Sukontharangsri Y; Chamnanvanakij S; Torcharus K; Viprakasit V Ann Clin Biochem; 2014 Mar; 51(Pt 2):237-47. PubMed ID: 23901141 [TBL] [Abstract][Full Text] [Related]
11. Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India. Phanasgaonkar S; Colah R; Ghosh K; Mohanty D; Gupte S Br J Biomed Sci; 2007; 64(4):160-3. PubMed ID: 18236737 [TBL] [Abstract][Full Text] [Related]
12. Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon. Zago MA; Costa FF; Bottura C J Med Genet; 1982 Dec; 19(6):437-40. PubMed ID: 7154040 [TBL] [Abstract][Full Text] [Related]
13. Complete suppression of haemoglobin A synthesis in haemoglobin D Los Angeles--beta thalassaemia. Marengo-Rowe AJ; McCracken AW; Flanagan P J Clin Pathol; 1968 Jul; 21(4):508-10. PubMed ID: 5697353 [TBL] [Abstract][Full Text] [Related]
15. [Analysis of a program for atypical familial microcytosis. Molecular basis of alpha-thalassemia]. Villegas Martínez A Sangre (Barc); 1990 Aug; 35(4):277-88. PubMed ID: 2274839 [TBL] [Abstract][Full Text] [Related]
16. Interaction between beta-thalassaemia and Hb G Philadelphia associated with alpha-thalassaemia. Stathopoulou R; Sulis E; Lehmann H Acta Haematol; 1979; 62(2):106-11. PubMed ID: 119398 [TBL] [Abstract][Full Text] [Related]
18. Interaction of Hb A2 Indonesia trait with beta-thalassaemia trait and with Hb E trait. Ganesan J; Lie-Injo LE Acta Haematol; 1978; 59(6):341-7. PubMed ID: 97892 [TBL] [Abstract][Full Text] [Related]
19. Modification of hemoglobin H disease by sickle trait. Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366 [TBL] [Abstract][Full Text] [Related]
20. Haemoglobin synthesis in alpha-thalassaemia (haemoglobin H disease). Clegg JB; Weatherall DJ Nature; 1967 Sep; 215(5107):1241-3. PubMed ID: 6052721 [No Abstract] [Full Text] [Related] [Next] [New Search]