1148 related articles for article (PubMed ID: 479366)
21. Clinical phenotypes and genotypes diagnosis of thalassemia in children.
Torcharus K; Sriphaisal T; Krutvecho T; Suwanasophon C; Intarapakawong J
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():275-7. PubMed ID: 8629123
[TBL] [Abstract][Full Text] [Related]
22. A study on the biochemical genetics of abnormal hemoglobins.
I-Tao T
Sci Sin; 1975; 18(4):527-44. PubMed ID: 1202635
[TBL] [Abstract][Full Text] [Related]
23. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
Adams JG; Boxer LA; Baehner RL; Forget BG; Tsistrakis GA; Steinberg MH
J Clin Invest; 1979 May; 63(5):931-8. PubMed ID: 447835
[TBL] [Abstract][Full Text] [Related]
24. The association of Hb Stanleyville II with alpha thalassemia and Hb S.
Costa FF; Zago MA; Sonati MF; Bottura C
Nouv Rev Fr Hematol (1978); 1987; 29(6):387-90. PubMed ID: 3452204
[TBL] [Abstract][Full Text] [Related]
25. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.
Singsanan S; Karnpean R; Fucharoen G; Sanchaisuriya K; Sae-Ung N; Fucharoen S
Blood Cells Mol Dis; 2010 Oct; 45(3):210-4. PubMed ID: 20615730
[TBL] [Abstract][Full Text] [Related]
26. Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family.
Felice AE; Mayson SM; Webber BB; Miller A; Gravely ME; Huisman TH
Pediatr Res; 1980 Mar; 14(3):266-7. PubMed ID: 7383748
[TBL] [Abstract][Full Text] [Related]
27. Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.
Lie-Injo LE; Hassan K; Joishy SK; Lim ML
Am J Hematol; 1986 Jul; 22(3):265-74. PubMed ID: 2424302
[TBL] [Abstract][Full Text] [Related]
28. Identification of a nondeletion defect in alpha-thalassemia.
Kan YW; Dozy AM; Trecartin R; Todd D
N Engl J Med; 1977 Nov; 297(20):1081-4. PubMed ID: 909565
[TBL] [Abstract][Full Text] [Related]
29. Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
Embury SH; Dozy AM; Miller J; Davis JR; Kleman KM; Preisler H; Vichinsky E; Lande WN; Lubin BH; Kan YW; Mentzer WC
N Engl J Med; 1982 Feb; 306(5):270-4. PubMed ID: 6172710
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
Zanella-Cleon I; Préhu C; Joly P; Riou J; Becchi M; Wajcman H; Francina A
Hemoglobin; 2009; 33(3):177-87. PubMed ID: 19657831
[TBL] [Abstract][Full Text] [Related]
32. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.
Wood WG; Stamatoyannopoulos G
J Clin Invest; 1975 Mar; 55(3):567-78. PubMed ID: 1167870
[TBL] [Abstract][Full Text] [Related]
33. Heterogeneity of DNA fragments associated with the sickle-globin gene.
Feldenzer J; Mears JG; Burns AL; Natta C; Bank A
J Clin Invest; 1979 Sep; 64(3):751-5. PubMed ID: 468989
[TBL] [Abstract][Full Text] [Related]
34. First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
Upadhye DS; Jain D; Nair SB; Nadkarni AH; Ghosh K; Colah RB
J Clin Pathol; 2012 Jul; 65(7):654-9. PubMed ID: 22461654
[TBL] [Abstract][Full Text] [Related]
35. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
Wong SC; Ali MA; Boyadjian SE
Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216
[TBL] [Abstract][Full Text] [Related]
36. Alpha thalassaemia in adults with sickle-cell trait.
Steinberg MH; Adams JG; Dreiling BJ
Br J Haematol; 1975 May; 30(1):31-7. PubMed ID: 1191571
[TBL] [Abstract][Full Text] [Related]
37. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.
Witkowska HE; Lubin BH; Beuzard Y; Baruchel S; Esseltine DW; Vichinsky EP; Kleman KM; Bardakdjian-Michau J; Pinkoski L; Cahn S
N Engl J Med; 1991 Oct; 325(16):1150-4. PubMed ID: 1891024
[No Abstract] [Full Text] [Related]
38. Alpha-thalassemia in premature newborns.
Maccioni L; Galanello R; Ruggeri R; Puddu R; Rosatelli D; Marras A; Chiappe S; Macciotta A; Cao A
Pediatr Res; 1986 Nov; 20(11):1077-81. PubMed ID: 3797101
[TBL] [Abstract][Full Text] [Related]
39. Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system.
Munkongdee T; Pichanun D; Butthep P; Klamchuen S; Chalermpolprapa V; Winichagoon P; Svasti S; Fucharoen S
Ann Hematol; 2011 Jul; 90(7):741-6. PubMed ID: 21188378
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
