145 related articles for article (PubMed ID: 6322098)
1. Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
Galanello R; Melis MA; Maccioni L; Pirastu M; Cao A
Pediatr Res; 1984 Feb; 18(2):158-62. PubMed ID: 6322098
[TBL] [Abstract][Full Text] [Related]
2. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
Lie-Injo LE; Herrera AR; Lebo RV; Hassan K; Lopez CG
Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
Pressley L; Higgs DR; Clegg JB; Weatherall DJ
Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3586-9. PubMed ID: 6158051
[TBL] [Abstract][Full Text] [Related]
5. A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease.
Fei YJ; Liu JC; Walker EL; Huisman TH
Am J Hematol; 1992 Apr; 39(4):299-300. PubMed ID: 1553958
[TBL] [Abstract][Full Text] [Related]
6. Alpha globin gene analysis in a Sardinian family with interacting alpha and beta thalassaemia genes.
Melis MA; Galanello R; Cao A
Br J Haematol; 1983 Apr; 53(4):667-71. PubMed ID: 6299325
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Characterization of a new alpha-thalassemia-1 deletion in a Spanish family.
Gonzalez-Redondo JM; Gilsanz F; Ricard P
Hemoglobin; 1989; 13(2):103-16. PubMed ID: 2544542
[TBL] [Abstract][Full Text] [Related]
9. Alpha-gene deletions in black newborn infants with Hb Bart's.
Ohene-Frempong K; Rappaport E; Atwater J; Schwartz E; Surrey S
Blood; 1980 Nov; 56(5):931-3. PubMed ID: 7426755
[TBL] [Abstract][Full Text] [Related]
10. Hb Bart's level in cord blood and deletions of alpha-globin genes.
Lie-Injo LE; Solai A; Herrera AR; Nicolaisen L; Kan YW; Wan WP; Hasan K
Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Modification of hemoglobin H disease by sickle trait.
Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
[TBL] [Abstract][Full Text] [Related]
13. Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.
Horst J; Griese EU; Kleihauer E; Kohne E
Hum Genet; 1984; 68(3):260-3. PubMed ID: 6094337
[TBL] [Abstract][Full Text] [Related]
14. Alpha thalassaemia in an Italian population.
Velati C; Sampietro M; Biassoni M; Cappellini MD; Wainscoat JS; Higgs DR; Fiorelli G
Br J Haematol; 1986 Jul; 63(3):497-501. PubMed ID: 3755350
[TBL] [Abstract][Full Text] [Related]
15. Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
Embury SH; Lebo RV; Dozy AM; Kan YW
J Clin Invest; 1979 Jun; 63(6):1307-10. PubMed ID: 447845
[TBL] [Abstract][Full Text] [Related]
16. The molecular basis of AE-Bart's disease.
Thonglairuam V; Winichagoon P; Fucharoen S; Wasi P
Hemoglobin; 1989; 13(2):117-24. PubMed ID: 2737907
[TBL] [Abstract][Full Text] [Related]
17. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
Bowden DK; Hill AV; Higgs DR; Oppenheimer SJ; Weatherall DJ; Clegg JB
J Clin Invest; 1987 Jan; 79(1):39-43. PubMed ID: 3793931
[TBL] [Abstract][Full Text] [Related]
18. Molecular pathology of haemoglobin H disease in Sardinians.
Paglietti E; Galanello R; Moi P; Pirastu M; Cao A
Br J Haematol; 1986 Jul; 63(3):485-96. PubMed ID: 3015190
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Influence of two alpha-globin gene deletions on homozygous beta 0-thalassemia.
Lie-Injo LE; Duraisamy G; Vasudevan S
Hemoglobin; 1982; 6(2):115-29. PubMed ID: 7096103
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
