154 related articles for article (PubMed ID: 4516146)
21. A new type of hereditary persistence of foetal haemoglobin: is a diffusible factor regulating gamma-chain synthesis?
Martinez G; Colombo B
Nature; 1974 Dec; 252(5485):735-6. PubMed ID: 4437631
[No Abstract] [Full Text] [Related]
22. Survey of Haryana children for abnormal hemoglobins.
Aggarwal VP; Dhatt PS; Singh H
Indian Pediatr; 1983 Apr; 20(4):255-8. PubMed ID: 6194111
[No Abstract] [Full Text] [Related]
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. [Genetic and hematological study of a family from Ghana suffering from hereditary persistence of fetal hemoglobin associated with beta-thalassemia and hemoglobinosis S].
Boreux G; Wyss M; Farquet JJ
Arch Genet (Zur); 1973; 46(1):22-33. PubMed ID: 4731929
[No Abstract] [Full Text] [Related]
25. Family with hereditary persistence of foetal haemoglobin.
Boon WH
Med J Malaya; 1968 Sep; 23(1):61-6. PubMed ID: 4237561
[No Abstract] [Full Text] [Related]
26. Haemoglobin synthesis during human fetal development.
Wood WG
Br Med Bull; 1976 Sep; 32(3):282-7. PubMed ID: 788839
[No Abstract] [Full Text] [Related]
27. A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.
Di Iorio EE; Winterhalter KH; Wilson K; Rosenmund A; Marti HR
Blut; 1975 Aug; 31(2):61-8. PubMed ID: 1164567
[TBL] [Abstract][Full Text] [Related]
28. Evidence for multiple structural genes for the gamma-chain of human fetal hemoglobin in hereditary persistence of fetal hemoglobin.
Huisman TH; Schroeder WA; Dozy AM; Shelton JR; Shelton JB; Boyd EM; Apell G
Ann N Y Acad Sci; 1969 Nov; 165(1):320-31. PubMed ID: 5260154
[No Abstract] [Full Text] [Related]
29. [Hemoglobin of the African newborn infant. Results of an investigation in Senegal].
Oudart JL; Diadhiou F; Sarrat H; Satgé P
Ann Pediatr (Paris); 1968 Dec; 15(12):773-81. PubMed ID: 4894442
[No Abstract] [Full Text] [Related]
30. Futher investigations of the gamma-chaina in a ghanaian adult, homozygous for hereditary perisitence of fetal haemoglobin. Isolation of gamma CB-3 peptides and Ggamma:Agamma ratio determination in human Hb E.
Kamuzora H; Ringelhann B; Konotey-Ahulu FI; Lehmann H; Lorkin PA
Acta Haematol; 1975; 53(5):315-20. PubMed ID: 808072
[TBL] [Abstract][Full Text] [Related]
31. Recent developments in foetal haemoglobin research.
Kamuzora H
Humangenetik; 1975 Sep; 30(3):197-205. PubMed ID: 1102427
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. The haemoglobinopathies.
Bird GW
Br Med J; 1972 Feb; 1(5796):363-8. PubMed ID: 4550414
[No Abstract] [Full Text] [Related]
34. Occurrence of haemoglobin Norfolk (alpha2 57 (E6) Gly leads to Asp beta2) at the level of 33% in an Italian family from Calabria.
Marinucci M; Mavilio F; Samoggia P; Tentori L; Spadea G; Cocone G
Acta Haematol; 1979; 61(1):39-46. PubMed ID: 105539
[TBL] [Abstract][Full Text] [Related]
35. Relation of beta to gamma synthesis during the first trimester: an approach to prenatal diagnosis of thalassemia.
Cividalli G; Nathan DG; Kan YW; Santamarina B; Frigoletto F
Pediatr Res; 1974 May; 8(5):553-60. PubMed ID: 4825524
[No Abstract] [Full Text] [Related]
36. Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathies.
Kazazian HH; Kaback MM; Woodhead AP; Leonard CO; Nersesian WS
Adv Exp Med Biol; 1972; 28():337-46. PubMed ID: 5085176
[No Abstract] [Full Text] [Related]
37. Haemoglobin P-Nilotic containing a - chain.
Badr FM; Lorkin PA; Lehmann H
Nat New Biol; 1973 Mar; 242(117):107-10. PubMed ID: 4513408
[No Abstract] [Full Text] [Related]
38. Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults.
Altay G; Garver F; Bannister WH; Grech JL; Felice A; Huisman TH
Biochem Genet; 1977 Oct; 15(9-10):915-23. PubMed ID: 588240
[TBL] [Abstract][Full Text] [Related]
39. Haemoglobinopathies in Burma. II. Haemoglobin H disease.
Aung-Than-Batu ; U-Hla-Pe ; Khin-Kyi-Nyunt
Trop Geogr Med; 1971 Mar; 23(1):19-23. PubMed ID: 4252406
[No Abstract] [Full Text] [Related]
40. The human fetal hemoglobins.
Huisman TH
Tex Rep Biol Med; 1980-1981; 40():29-42. PubMed ID: 6172867
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
