Zobrazeno 1 - 10
of 49
pro vyhledávání: '"T. A. Stoming"'
Autor:
E. George, T. A. Stoming, G. Petkov, K. G. Yang, Titus H.J. Huisman, L. Jankovic, Georgi D. Efremov, Christos Kattamis
Publikováno v:
British Journal of Haematology. 75:122-126
In an ongoing effort to identify point mutations causing beta-thalassaemia, we have found two previously unreported mutations which are located in the Poly A site of the beta-globin gene. The screening programme used amplified DNA and dot-blot hybrid
Autor:
Ralph L. Elkins, You-Jung Fei, Jeffrey L. Rausch, Gaylon L. Edwards, T. A. Stoming, Jerry J. Buccafusco, T. Edward Orr, Stephen H. Hobbs, G.Frank Carl
Publikováno v:
Annals of the New York Academy of Sciences. 985:519-521
Autor:
V. R. Arruda, J.F. Nechtman, Goncalves, M Kimura, T. A. Stoming, Maria de Fátima Sonati, F. F. Costa
Publikováno v:
Hemoglobin. 18:235-239
(1994). Association of Hb santa ANA [α2β288(F4)LEU→PRO] And Hb porto alegre [α2β29(A6)SER→CYS] in a brazilian female. Hemoglobin: Vol. 18, No. 3, pp. 235-239.
Publikováno v:
Hemoglobin. 17:563-567
(1993). A Novel β-Thalassemia Mutation [IVS-II-5 (G→C)] in a Chinese Family from Guangxi Province, P. R. China. Hemoglobin: Vol. 17, No. 6, pp. 563-567.
Autor:
R. Öner, Yurdanur Kilinç, Muzaffer Aksoy, Abdullah Kutlar, Titus H.J. Huisman, A. L. Reese, Cigdem Altay, T. A. Stoming, Aytemiz Gurgey, Ferdane Kutlar
Publikováno v:
Hemoglobin. 14:1-13
A review is presented of the various beta-thalassemia alleles observed in nearly 191 patients with beta-thalassemia major and their 182 heterozygous relatives. Determination was by gene amplification and dot-blot hybridization with synthetic probes,
Autor:
M S, Goncalves, J F, Nechtman, M S, Figueiredo, J, Kerbauy, V R, Arruda, M F, Sonati, S O, Saad, F F, Costa, T A, Stoming
Publikováno v:
Human heredity. 44(6)
In this study we have determined the frequency of beta S haplotypes in a Brazilian sickle cell disease population from Sao Paulo, Brazil, by analyzing sequence variations in the immediate 5' flanking and second intervening sequence (IVSII) regions of
Publikováno v:
Hemoglobin. 18(3)
Autor:
Titus H.J. Huisman, X. J. Wen, J. F. Nechtman, J.-B. Zhao, N. H. Jiang, S. Liang, T. A. Stoming, R. Liang
Publikováno v:
British journal of haematology. 86(2)
We have studied nearly 100 patients with beta-thalassaemia major and 60 patients with Hb H disease who were attending the Haematology Clinic of Guangxi Medical College. Treatment of the patients was limited and only a few patients with beta-thalassae
Autor:
L. Jankovic, G. D. Efremov, G. Petkov, C. Kattamis, E. George, K-G. Yang, T. A. Stoming, T. H. J. Huisman
Publikováno v:
British journal of haematology. 75(1)
In an ongoing effort to identify point mutations causing beta-thalassaemia, we have found two previously unreported mutations which are located in the Poly A site of the beta-globin gene. The screening programme used amplified DNA and dot-blot hybrid
Autor:
R, Oner, C, Altay, A, Gurgey, M, Aksoy, Y, Kilinç, T A, Stoming, A L, Reese, A, Kutlar, F, Kutlar, T H, Huisman
Publikováno v:
Hemoglobin. 14(1)
A review is presented of the various beta-thalassemia alleles observed in nearly 191 patients with beta-thalassemia major and their 182 heterozygous relatives. Determination was by gene amplification and dot-blot hybridization with synthetic probes,