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23. Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin. Chui DH; Patterson M; Dowling CE; Kazazian HH; Kendall AG N Engl J Med; 1990 Jul; 323(3):179-82. PubMed ID: 1694572 [No Abstract] [Full Text] [Related]
24. [Increasing number of hemoglobinopathies. Rapid diagnosis with DNA technique]. Bui TH; Anvret M; Bröndum-Nielsen K Lakartidningen; 1992 Sep; 89(39):3174, 3177. PubMed ID: 1405929 [No Abstract] [Full Text] [Related]
25. Prenatal diagnosis of hemoglobinopathies: evaluation of techniques for analysing globin-chain synthesis in blood samples obtained by fetoscopy. Congote LF; Hamilton EF; Chow JC; Perry TB Can Med Assoc J; 1982 Nov; 127(9):843-9. PubMed ID: 7139502 [TBL] [Abstract][Full Text] [Related]
26. [Molecular biology completes clinical chemical methods in investigation of hemoglobin diseases]. Landin B; Jeppsson JO Lakartidningen; 1992 Sep; 89(39):3147-8. PubMed ID: 1405918 [No Abstract] [Full Text] [Related]
28. [Childhood hemoglobinopathies]. Lambotte C Rev Med Liege; 1980 Apr; 35(7):221-34. PubMed ID: 7455462 [No Abstract] [Full Text] [Related]
29. [Hemoglobinopathies, screening and molecular-genetic studies in foreign women in The Netherlands]. Losekoot M; Fodde R; Giordano PC Ned Tijdschr Geneeskd; 1992 Jul; 136(30):1477-8. PubMed ID: 1369781 [No Abstract] [Full Text] [Related]
30. Pathophysiology of the hemoglobinopathies. Abel HR; Bradley TB; Ranney HM Clin Obstet Gynecol; 1969 Mar; 12(1):15-48. PubMed ID: 4894453 [No Abstract] [Full Text] [Related]
31. The molecular biology of the thalassemia syndromes. Bank A; Ramirez F CRC Crit Rev Biochem; 1978; 5(4):343-67. PubMed ID: 363354 [No Abstract] [Full Text] [Related]
32. Carrier screening for thalassemia and hemoglobinopathies in Canada. Langlois S; Ford JC; Chitayat D; ; J Obstet Gynaecol Can; 2008 Oct; 30(10):950-959. PubMed ID: 19038079 [TBL] [Abstract][Full Text] [Related]
33. Molecular pathology of disorders of hemoglobin. Bank A; Ramirez F Pathobiol Annu; 1976; 6():95-118. PubMed ID: 798166 [No Abstract] [Full Text] [Related]
34. Forty-four years (1955-1999) devoted to hemoglobin research: Titus H. J. Huisman (1923-1999). Efremov GD Hemoglobin; 2001 May; 25(2):125-68. PubMed ID: 11480778 [No Abstract] [Full Text] [Related]
35. Hemoglobinopathies and thalassemias. Abnormalities of hemoglobin structure, function, and synthesis. Honig GR Postgrad Med; 1974 May; 55(5):77-83. PubMed ID: 4596320 [No Abstract] [Full Text] [Related]
37. [Current status of the study of hemoglobinopathies in Costa Rica]. Sáenz GF Sangre (Barc); 1985; 30(2):168-80. PubMed ID: 4012518 [No Abstract] [Full Text] [Related]
38. The normal hemoglobins and the hemoglobinopathies: background. Pauling L Tex Rep Biol Med; 1980-1981; 40():1-7. PubMed ID: 7034263 [No Abstract] [Full Text] [Related]
39. [Heterozygous beta thalassemia with increased HbF: independent segregation of beta thalassemia and hereditary persistent fetal hemoglobin (Swiss type) in a Spanish family]. De Blas JM; Martín E; Martínez ML; Caso F Sangre (Barc); 1985; 30(1):28-36. PubMed ID: 2408346 [No Abstract] [Full Text] [Related]
40. Genetic disorders of hemoglobin synthesis. Bank A Hosp Pract (Off Ed); 1985 Sep; 20(9):109-11, 115-9, 123-4. PubMed ID: 2411743 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]