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24. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system. Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525 [TBL] [Abstract][Full Text] [Related]
25. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies. Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028 [TBL] [Abstract][Full Text] [Related]
26. Genetic and molecular diversity in nondeletion Hb H disease. Higgs DR; Pressley L; Aldridge B; Clegg JB; Weatherall DJ; Cao A; Hadjiminas MG; Kattamis C; Metaxatou-Mavromati A; Rachmilewitz EA; Sophocleous T Proc Natl Acad Sci U S A; 1981 Sep; 78(9):5833-7. PubMed ID: 6272319 [TBL] [Abstract][Full Text] [Related]
27. Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat. Nicholls RD; Higgs DR; Clegg JB; Weatherall DJ Blood; 1985 Jun; 65(6):1434-8. PubMed ID: 2986746 [TBL] [Abstract][Full Text] [Related]
28. Molecular basis of hemoglobin-H disease in the Mediterranean population. Kan YW; Dozy AM; Stamatoyannopoulos G; Hadjiminas MG; Zachariades Z; Furbetta M; Cao A Blood; 1979 Dec; 54(6):1434-8. PubMed ID: 508946 [TBL] [Abstract][Full Text] [Related]
30. Relative numbers of human globin genes assayed with purified alpha and beta complementary human DNA. Ramirez F; Natta C; O'Donnell JV; Canale V; Bailey G; Sanguensermsri T; Maniatis GM; Marks PA; Bank A Proc Natl Acad Sci U S A; 1975 Apr; 72(4):1550-4. PubMed ID: 1055426 [TBL] [Abstract][Full Text] [Related]
31. Delta-beta-thalassemia is due to a gene deletion. Ottolenghi S; Comi P; Giglioni B; Tolstoshev P; Lanyon WG; Mitchell GJ; Williamson R; Russo G; Musumeci S; Schillro G; Tsistrakis GA; Charache S; Wood WG; Clegg JB; Weatherall DJ Cell; 1976 Sep; 9(1):71-80. PubMed ID: 975241 [TBL] [Abstract][Full Text] [Related]
32. Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia. Honig GR; Shamsuddin M; Vida LN; Mompoint M; Valcourt E; Bowie LJ; Jones EC; Powers PA; Spritz RA; Guis M J Clin Invest; 1984 Jun; 73(6):1740-9. PubMed ID: 6725558 [TBL] [Abstract][Full Text] [Related]
33. Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype. Galanello R; Paglietti E; Melis MA; Giagu L; Cao A Acta Haematol; 1984; 72(1):34-6. PubMed ID: 6089487 [TBL] [Abstract][Full Text] [Related]
34. Molecular genetics of human hemoglobin synthesis. Forget BG Ann Intern Med; 1979 Oct; 91(4):605-16. PubMed ID: 384860 [TBL] [Abstract][Full Text] [Related]
35. Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence? Weatherall DJ; Higgs DR; Bunch C; Old JM; Hunt DM; Pressley L; Clegg JB; Bethlenfalvay NC; Sjolin S; Koler RD; Magenis E; Francis JL; Bebbington D N Engl J Med; 1981 Sep; 305(11):607-12. PubMed ID: 6267462 [TBL] [Abstract][Full Text] [Related]
36. Mapping the alpha-globin genes in an Algerian HbH patient and his family. Whitelaw E; Pagnier J; Verdier G; Henni T; Godet J; Williamson R Blood; 1980 Mar; 55(3):511-6. PubMed ID: 7357081 [TBL] [Abstract][Full Text] [Related]
37. Homozygous alpha thalassemia/Hb G Philadelphia. Pardoll DM; Charache S; Hjelle BL; Jones R; Phillips JA; Smith RR; Rodeheffer RJ Hemoglobin; 1982; 6(5):503-15. PubMed ID: 6294002 [TBL] [Abstract][Full Text] [Related]
38. Molecular pathology of alpha-thalassemia. Kan YW Ann N Y Acad Sci; 1985; 445():28-36. PubMed ID: 3860131 [TBL] [Abstract][Full Text] [Related]
39. The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease. Orkin SH; Old J; Lazarus H; Altay C; Gurgey A; Weatherall DJ; Nathan DG Cell; 1979 May; 17(1):33-42. PubMed ID: 455460 [TBL] [Abstract][Full Text] [Related]
40. Alpha zero- and beta zero-thalassemia in a Thai family: unusually mild homozygous beta zero-thalassemia without alpha-globin gene deletion. Yenchitsomanus P; Summers KM Hum Genet; 1985; 69(4):375-7. PubMed ID: 2580774 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]