AMPLIFICAÇÃO GÊNICA ALELO ESPECÍFICA E MULTIPLEX NO DIAGNÓSTICO LABORATORIAL DE HEMOGLOBINAS ANORMAIS

作者: Luciane Cristina Bertholo

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参考文章(119)
M. F. Sonati, E. M. Kimura, H. Z. W. Grotto, S. A. Gervasio, F. F. Costa, Hereditary Hemoglobinopathies in a Population from so Hemoglobin. ,vol. 20, pp. 175- 179 ,(1996) , 10.3109/03630269609027926
SRP Miranda, MS Figueiredo, J Kerbauy, HZW Grotto, STO Saad, FF Costa, None, Hb LeporeBaltimoreδ5OSer β86Ala) Identified by DNA Analysis in a Brazilian Family Acta Haematologica. ,vol. 91, pp. 7- 9 ,(1994) , 10.1159/000204252
Renzo Galanello, Carla Sollaino, Elisabetta Paglietti, Susanna Barella, Chiara Perra, Ilaria Doneddu, Maria G. Pirroni, Liliana Maccioni, Antonio Cao, α-thalassemia carrier identification by DNA analysis in the screening for thalassemia American Journal of Hematology. ,vol. 59, pp. 273- 278 ,(1998) , 10.1002/(SICI)1096-8652(199812)59:4<273::AID-AJH2>3.0.CO;2-3
J. B. CLEGG, D. J. WEATHERALL, P. F. MILNER, Haemoglobin Constant Spring—A Chain Termination Mutant ? Nature. ,vol. 234, pp. 337- 340 ,(1971) , 10.1038/234337A0
Andreas E. Kulozik, John Lyons, Elisabeth Kohne, Claus R. Bartram, Enno Kleihauer, Rapid and non-radioactive prenatal diagnosis of β thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR) British Journal of Haematology. ,vol. 70, pp. 455- 458 ,(1988) , 10.1111/J.1365-2141.1988.TB02516.X
Richard M Lawn, Argiris Efstratiadis, Catherine O'Connell, Tom Maniatis, The nucleotide sequence of the human β-globin gene Cell. ,vol. 21, pp. 647- 651 ,(1980) , 10.1016/0092-8674(80)90428-6
A. Ashley-Koch, Q. Yang, R. S. Olney, Sickle Hemoglobin (Hb S) Allele and Sickle Cell Disease: A HuGE Review American Journal of Epidemiology. ,vol. 151, pp. 839- 845 ,(2000) , 10.1093/OXFORDJOURNALS.AJE.A010288
Linus Pauling, Sickle Cell Anemia, a Molecular Disease Science. ,vol. 110, pp. 543- 548 ,(1949) , 10.1126/SCIENCE.110.2865.543
K. L. Harteveld, Monique Losekoot, Angelien J. G. A. M. Heister, Michiel van der Wielen, Piero C. Giordano, Luigi F. Bernini, alpha-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutations Human Genetics. ,vol. 100, pp. 465- 471 ,(1997) , 10.1007/S004390050535
R. Saiki, D. Gelfand, S Stoffel, S. Scharf, R Higuchi, G. Horn, K. Mullis, H. Erlich, Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase Science. ,vol. 239, pp. 487- 491 ,(1988) , 10.1126/SCIENCE.2448875