Hb Campinas [α26(b7)ala → Val]: A Novel, Electrophoretically Silent, Variant

dc.creatorWenning M.R.S.C.
dc.creatorSilva N.M.
dc.creatorJorge S.B.
dc.creatorKimura E.M.
dc.creatorCosta F.F.
dc.creatorTorsoni M.A.
dc.creatorOgo S.H.
dc.creatorSonati M.D.F.
dc.date2000
dc.date2015-06-30T19:49:15Z
dc.date2015-11-26T14:46:39Z
dc.date2015-06-30T19:49:15Z
dc.date2015-11-26T14:46:39Z
dc.date.accessioned2018-03-28T21:56:30Z
dc.date.available2018-03-28T21:56:30Z
dc.identifier
dc.identifierHemoglobin. , v. 24, n. 2, p. 143 - 148, 2000.
dc.identifier3630269
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0033623698&partnerID=40&md5=d85955f61100ada61ae78665f28e70b5
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/107091
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/107091
dc.identifier2-s2.0-0033623698
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1252932
dc.description[No abstract available]
dc.description24
dc.description2
dc.description143
dc.description148
dc.descriptionBunn, H.F., Forget, B.G., (1986) Hemoglobin: Molecular, Genetic and Clinical Aspects, , W.B. Saunders Company, Philadelphia, PA, USA
dc.descriptionMoo-Penn, W.F., Jue, D.L., Johnson, M.H., Bechtel, K.C., Patchen, L.C., Hemoglobin variants and methods used for their characterization during 7 years of screening at the Center for Disease Control (1980) Hemoglobin, 4, pp. 347-361
dc.descriptionDacie, J.V., Lewis, S.M., (1995) Practical Haematology, 8 th Edition, , Churchill Livingstone, London, England
dc.descriptionAlter, B.P., Goff, S.C., Efremov, G.D., Gravely, M.E., Huisman, T.H.J., Globin chain electrophoresis: A new approach to the determination of the Gγ/ Aγ ratio of globin synthesis (1980) Br. J. Haematol., 44, pp. 527-534
dc.descriptionPembrey, M.E., MacWade, P., Weatherall, D.J., Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation (1972) J. Clin. Pathol., 25, pp. 738-740
dc.descriptionBlouquit, Y., Braconnier, F., Cohen-Solal, M., Foldi, J., Arous, N., Ankri, A., Binet, J.L., Rosa, J., Hemoglobin Pitie-Salpetriere [β34 (B16) Val → Phe] a new high oxygen affinity variant associated with familial erythrocytosis (1980) Biochim. Biophys. Acta, 624, pp. 473-478
dc.descriptionDodé, C., Rochette, J., Krishnamoorthy, R., Locus assignment of human α globin mutations by selective amplification and direct sequencing (1990) Br. J. Haematol., 76, pp. 275-281
dc.descriptionSanger, F., Nickelen, S., Coulson, A.R., DNA sequencing with chain terminating inhibitors (1977) Proc. Natl. Acad Sci. USA, 74, pp. 5463-5467
dc.descriptionThein, S.L., Hinton, J., A simple and rapid method of direct sequencing using Dynabeads (1991) Br. J. Haematol., 79, pp. 113-115
dc.descriptionBaysal, E., Huisman, T.H.J., Detection of common deletional α-thalassemia-2 determinants by PCR (1994) Am. J. Haematol., 46, pp. 208-213
dc.descriptionDodé, C., Krishnamoorthy, R., Lamb, J., Rochette, J., Rapid analysis of -α 3.7 thalassaemia and ααα anti 3.7 triplication by enzymatic amplification analysis (1992) Br. J. Haematol., 82, pp. 105-111
dc.descriptionZeng, Y.-T., Huang, S.-Z., Zhou, X.-D., Qui, X.-K., Dong, Q.-Y., Li, M.-Y., Bai, J.-H., Hb Shenyang [α26 (B7) Ala → Glu]: A new unstable variant found in China (1982) Hemoglobin, 6, pp. 625-628
dc.descriptionLacerra, G., De Angioletti, M., Di Girolamo, R., Sciorio, A., Testa, R., Schilirò, G., Carestia, C., Hb Caserta and Hb Bronte: Two novel hemoglobin variants caused by alpha-2 globin gene mutation (1997) The 6th International Conference on Thalassaemia and the Haemoglobinopathies, , Abstract 151, Malta, April
dc.languageen
dc.publisher
dc.relationHemoglobin
dc.rightsfechado
dc.sourceScopus
dc.titleHb Campinas [α26(b7)ala → Val]: A Novel, Electrophoretically Silent, Variant
dc.typeArtículos de revistas


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