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7. Globin synthesis in alpha- and beta-thalassemia. Ramot B; Ben-Bassat I; Mozel M; Shacked N Isr J Med Sci; 1973; 9(9):1469-74. PubMed ID: 4359643 [No Abstract] [Full Text] [Related]
8. Hemoglobinopathies among five major ethnic groups in Karachi, Pakistan. Ghani R; Manji MA; Ahmed N Southeast Asian J Trop Med Public Health; 2002 Dec; 33(4):855-61. PubMed ID: 12757239 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Childhood hemoglobinopathies]. Lambotte C Rev Med Liege; 1980 Apr; 35(7):221-34. PubMed ID: 7455462 [No Abstract] [Full Text] [Related]
11. [Current status of the problem of abnormal hemoglobins. Preliminary reflexions]. Rosa J Nouv Rev Fr Hematol; 1971; 11(1):27-31. PubMed ID: 4252103 [No Abstract] [Full Text] [Related]
12. Recombinant deoxyribonucleic acid and the study of human genetic disease: the haemoglobinopathies. Little PF; Kooter JM; De Boer E; Annison G; Flavell RA Biochem Soc Symp; 1979; 44():57-64. PubMed ID: 496995 [No Abstract] [Full Text] [Related]
13. Frequency of sickling disorders in U.S. blacks. Motulsky AG N Engl J Med; 1973 Jan; 288(1):31-3. PubMed ID: 4681897 [No Abstract] [Full Text] [Related]
14. The molecular genetics of the thalassemia syndromes. Benz EJ; Forget BG Prog Hematol; 1975; 9():107-55. PubMed ID: 766070 [No Abstract] [Full Text] [Related]
15. Regulation of hemoglobin synthesis during the development of the red cell (third of three parts). Nienhuis AW; Benz EJ N Engl J Med; 1977 Dec; 297(26):1430-6. PubMed ID: 337141 [TBL] [Abstract][Full Text] [Related]
16. Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns; haemoglobin F Dickinson (Agamma97His-Arg), a new variant. Schneider RG; Haggard ME; Gustavson LP; Brimhall B; Jones RT Br J Haematol; 1974 Dec; 28(4):515-24. PubMed ID: 4455303 [No Abstract] [Full Text] [Related]
17. Student screening for inherited blood disorders in Bahrain. Al-Arrayed S; Hafadh N; Amin S; Al-Mukhareq H; Sanad H East Mediterr Health J; 2003 May; 9(3):344-52. PubMed ID: 15751927 [TBL] [Abstract][Full Text] [Related]
18. Incidence of haemoglobinopathies detected through neonatal screening in the United Arab Emirates. Al Hosani H; Salah M; Osman HM; Farag HM; Anvery SM East Mediterr Health J; 2005 May; 11(3):300-7. PubMed ID: 16602448 [TBL] [Abstract][Full Text] [Related]
19. [Consequences of the substitution of a single base in the genetic code]. Feo F Minerva Med; 1979 Mar; 70(11):823-7. PubMed ID: 431838 [No Abstract] [Full Text] [Related]
20. Disorders of the synthesis of human fetal hemoglobin. Manca L; Masala B IUBMB Life; 2008 Feb; 60(2):94-111. PubMed ID: 18379999 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]