91 related articles for article (PubMed ID: 3219296)
1. Characterization of a newly discovered alpha-thalassaemia-1 in two Spanish patients with Hb H disease.
Gonzalez-Redondo JM; Diaz-Chico JC; Malcorra-Azpiazu JJ; Balda-Aguirre MI; Huisman TH
Br J Haematol; 1988 Dec; 70(4):459-63. PubMed ID: 3219296
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation.
Yüregir GT; Aksoy K; Cürük MA; Dikmen N; Fei YJ; Baysal E; Huisman TH
Br J Haematol; 1992 Apr; 80(4):527-32. PubMed ID: 1581238
[TBL] [Abstract][Full Text] [Related]
5. Organization of the zeta-alpha genes in Chinese.
Chan V; Chan TK; Cheng MY; Kan YW; Todd D
Br J Haematol; 1986 Sep; 64(1):97-105. PubMed ID: 3756105
[TBL] [Abstract][Full Text] [Related]
6. A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian family.
Fortina P; Dianzani I; Serra A; Gottardi E; Saglio G; Farinasso L; Piga A; Gabutti V; Camaschella C
Br J Haematol; 1991 Aug; 78(4):529-34. PubMed ID: 1911344
[TBL] [Abstract][Full Text] [Related]
7. Characterization of a new alpha zero thalassaemia defect in the South African population.
Vandenplas S; Higgs DR; Nicholls RD; Bester AJ; Mathew CG
Br J Haematol; 1987 Aug; 66(4):539-42. PubMed ID: 3663510
[TBL] [Abstract][Full Text] [Related]
8. Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.
Fei YJ; Liu JC; Jogessar VB; Westermeyer KR; Bridgemohan R; Huisman TH
Acta Haematol; 1992; 87(1-2):11-5. PubMed ID: 1585766
[TBL] [Abstract][Full Text] [Related]
9. Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion.
Chui DH; Wong SC; Chung SW; Patterson M; Bhargava S; Poon MC
N Engl J Med; 1986 Jan; 314(2):76-9. PubMed ID: 3941693
[TBL] [Abstract][Full Text] [Related]
10. Identification of an extensive zeta-alpha globin gene deletion in a Chinese individual.
Waye JS; Eng B; Chui DH
Br J Haematol; 1992 Mar; 80(3):378-80. PubMed ID: 1581218
[TBL] [Abstract][Full Text] [Related]
11. A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns.
Fei YJ; Kutlar F; Harris HF; Wilson MM; Milana A; Sciacca P; Schiliro G; Masala B; Manca L; Altay C
Hemoglobin; 1989; 13(1):45-65. PubMed ID: 2703365
[TBL] [Abstract][Full Text] [Related]
12. Alpha thalassaemia in two Spanish families.
Villegas A; Calero F; Vickers MA; Ayyub H; Higgs DR
Eur J Haematol; 1990 Feb; 44(2):109-15. PubMed ID: 2318293
[TBL] [Abstract][Full Text] [Related]
13. [Analysis of a program for atypical familial microcytosis. Molecular basis for alpha-thalassemia. GEHBTA].
Sangre (Barc); 1990 Apr; 35(2):102-13. PubMed ID: 2363092
[TBL] [Abstract][Full Text] [Related]
14. The molecular basis of alpha thalassaemia in a South African population.
Mathew CG; Rousseau J; Rees JS; Harley EH
Br J Haematol; 1983 Sep; 55(1):103-11. PubMed ID: 6309210
[TBL] [Abstract][Full Text] [Related]
15. An elongated segment of DNA observed between two human alpha globin genes.
Nakatsuji T; Landman H; Huisman TH
Hum Genet; 1986 Dec; 74(4):368-71. PubMed ID: 3025076
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of a new family with alpha-thalassemia-1 (--MA mutation).
Villegas A; Sánchez J; Carreño DL; Ropero P; González FA; Espinós D; Peñalver MA; Lozano M
Am J Hematol; 1995 Aug; 49(4):294-8. PubMed ID: 7639274
[TBL] [Abstract][Full Text] [Related]
17. Characterization of an Indian (delta beta)0 thalassaemia.
Wainscoat JS; Old JM; Wood WG; Trent RJ; Weatherall DJ
Br J Haematol; 1984 Oct; 58(2):353-60. PubMed ID: 6477837
[TBL] [Abstract][Full Text] [Related]
18. (Alpha)alpha 5.3: a novel alpha(+)-thalassemia deletion with the breakpoints in the alpha 2-globin gene and in close proximity to an Alu family repeat between the psi alpha 2- and psi alpha 1-globin genes.
Lacerra G; Fioretti G; De Angioletti M; Pagano L; Guarino E; de Bonis C; Viola A; Maglione G; Scarallo A; De Rosa L
Blood; 1991 Nov; 78(10):2740-6. PubMed ID: 1824266
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Dysfunctional alpha-globin genes in hemoglobin H disease in blacks: variation in restriction fragment size permits the detection of the -alpha/-alpha T genotype.
Safaya S; Mullaney P; Rieder RF
Am J Hematol; 1987 Dec; 26(4):329-39. PubMed ID: 2891296
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
