261 related articles for article (PubMed ID: 3533181)
1. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.
Steinberg MH; Embury SH
Blood; 1986 Nov; 68(5):985-90. PubMed ID: 3533181
[TBL] [Abstract][Full Text] [Related]
2. Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene.
Steinberg MH; Embury SH
Birth Defects Orig Artic Ser; 1987; 23(5A):43-8. PubMed ID: 3689929
[No Abstract] [Full Text] [Related]
3. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
Steinberg MH; Coleman MB; Adams JG; Hartmann RC; Saba H; Anagnou NP
Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
[TBL] [Abstract][Full Text] [Related]
4. Association of Hb H disease with sickle-trait.
Martinez G; Ferreira R; Hernandez A; Di Rienzo A; Colombo B
Hemoglobin; 1986; 10(4):421-5. PubMed ID: 3744872
[No Abstract] [Full Text] [Related]
5. The leftward deletion alpha-thal-2 haplotype in a black subject with hemoglobin SS.
Embury SH; Gholson MA; Gillette P; Rieder RF
Blood; 1985 Mar; 65(3):769-71. PubMed ID: 3971048
[TBL] [Abstract][Full Text] [Related]
6. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
Honig GR; Gunay U; Mason RG; Vida LN; Ferenc C
Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
[TBL] [Abstract][Full Text] [Related]
7. Review: the sickle hemoglobinopathies--genetic analyses of common phenocopies and new molecular approaches to treatment.
Steinberg MH
Am J Med Sci; 1984 Nov; 288(4):169-74. PubMed ID: 6208780
[TBL] [Abstract][Full Text] [Related]
8. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
Raffield LM; Ulirsch JC; Naik RP; Lessard S; Handsaker RE; Jain D; Kang HM; Pankratz N; Auer PL; Bao EL; Smith JD; Lange LA; Lange EM; Li Y; Thornton TA; Young BA; Abecasis GR; Laurie CC; Nickerson DA; McCarroll SA; Correa A; Wilson JG; ; Lettre G; Sankaran VG; Reiner AP
PLoS Genet; 2018 Mar; 14(3):e1007293. PubMed ID: 29590102
[TBL] [Abstract][Full Text] [Related]
9. Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India.
Fodde R; Losekoot M; van den Broek MH; Oldenburg M; Rashida N; Schreuder A; Wijnen JT; Giordano PC; Nayudu NV; Khan PM
Hum Genet; 1988 Oct; 80(2):157-60. PubMed ID: 3169739
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.
Felice AE; Ozdonmez R; Headlee ME; Huisman TH
Biochem Genet; 1982 Aug; 20(7-8):689-701. PubMed ID: 6291506
[No Abstract] [Full Text] [Related]
13. Sickle cell-beta-thalassemia: a common phenocopy of sickle cell anemia.
Steinberg MH; Adams JG; Hendrix R
J Miss State Med Assoc; 1982 Nov; 23(11):319-21. PubMed ID: 7175930
[No Abstract] [Full Text] [Related]
14. Evolution of sickle variant gene.
Kurnit DM
Lancet; 1979 Jan; 1(8107):104. PubMed ID: 84107
[No Abstract] [Full Text] [Related]
15. Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes.
Embury SH; Clark MR; Monroy G; Mohandas N
J Clin Invest; 1984 Jan; 73(1):116-23. PubMed ID: 6690472
[TBL] [Abstract][Full Text] [Related]
16. Studies on sickle cell heterozygotes in Saudi Arabia--interaction with alpha-thalassaemia.
el-Hazmi MA
Acta Haematol; 1986; 75(2):100-4. PubMed ID: 3090815
[TBL] [Abstract][Full Text] [Related]
17. The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization?
Embury SH
Ann N Y Acad Sci; 1985; 445():37-44. PubMed ID: 3893275
[TBL] [Abstract][Full Text] [Related]
18. Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.
Shaeffer JR; DeSimone J; Kleve LJ
Biochem Genet; 1975 Dec; 13(11-12):783-8. PubMed ID: 1200978
[TBL] [Abstract][Full Text] [Related]
19. α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
Vayá A; Collado S; Alis R; Vera B; Romagnoli M; Barragán E
Hemoglobin; 2014; 38(3):165-8. PubMed ID: 24601859
[TBL] [Abstract][Full Text] [Related]
20. (delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell gene.
Trent RJ; Svirklys L; Harris MG; Hocking DR; Kronenberg H
Pathology; 1986 Jan; 18(1):117-22. PubMed ID: 2425331
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]