Fluorescence in Situ Hybridization (Fish) in Samples of Amniotic Fluid Obtained By Early Amniocentesis

Hibridación in Situ por Fluorescencia (Fish) en Muestras de Líquido Amniótico Obtenido por Amniocentesis Precoz

dc.creatorBernal Parra, Luz Mery
dc.creatorGollop, Thomaz Rafael
dc.creatorNaccache, Nadyr
dc.date.accessioned2019-11-08T21:24:49Z
dc.date.accessioned2022-09-28T12:21:05Z
dc.date.available2019-11-08T21:24:49Z
dc.date.available2022-09-28T12:21:05Z
dc.date.created2019-11-08T21:24:49Z
dc.identifierhttps://repository.unad.edu.co/handle/10596/29984
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3629989
dc.publisherUniversidad Colegio Mayor de Cundinamarca
dc.relationhttp://hemeroteca.unad.edu.co/index.php/nova/article/view/495/1068
dc.relation/*ref*/Klinger K., Landes G., Shook D., Harvey R., Lopez L., Locke P., Lerner T., Osathanondh R., Leverone B., Houseal T. (1992). Rapid detection of chromosome aneuploidies in uncultured amniocytes by using flourescence in situ hybridization. Am. J. Hum. Genet., 51:55-65.
dc.relation/*ref*/Jalal S.M., Law M.E., Carlson R.O., Dewald G.W. (1998). Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridization.Mayo.Clin. Proc., 73:132-137.
dc.relation/*ref*/Eiben B., Trawicki W., Hammans W., Goebel R., Epplen J.T. (1998). A prospective comparative study on fluorescence in situ hybridization (FlSH) of uncultured amniocytes and standard karyotype analysis. Prenat.Diagn., 18:901-906.
dc.relation/*ref*/Morris A., Boyd E., Dhanjal S., Lowther G.W., Aitken D.A., Young J., Menzies A., lmrie S.J., Connor J.M. (1999). Two years prospective experience using flourescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies. Prenat, Diagn, 19:546-551.
dc.relation/*ref*/WyandtHE,Tonk VS, Huang XL, Evans AT, Milunsky A. Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis. Fetal DiagnTher 2006; 21: 235-240.
dc.relation/*ref*/Ward B,E., Gersen S.L., Carelli M.P., McGuire N.M., Dackowski W.R., Weinstein M., Sandlin C., Warren R., Klinger K.W. (1993). Rapid prenatal diagnosis of chromosomal aneuploidies by flourescence in situ hybridization: clinical experience with 4500 specimens. Am. J. Hum. Genet, 52:854-865.
dc.relation/*ref*/D’AIton M‘, Malone F.D., Chelmow D., Ward B.E., Bianchi D.W. (1997).Defining the role of uorescense in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies. Am. J. Obstet. Gynecol., 176(4):769-776.
dc.relation/*ref*/Lewin P., Kleinfinger P., Bazin A., Mossafa H., Szpiro-Tapia S. (2000). Defining the efficiency of fluorescence in situ hybridization on uncultured amniocytes on a retrospective cohort of 27407 diagnosis. Prenat.Diagn., 20(1): 1-6.
dc.relation/*ref*/Thilaganathan B., Sairam S., Ballard T., Peterson C., Meredith R. (2000). Effectiveness of prenatal chromosomal analysis using multicolor fluorescet in situ hybridization. Br. J. Obstet. Gynaecol., 107(2):262-266.
dc.relation/*ref*/Chan-wei. Fluorescence in situ hybridization in uncultured amniocytesfor detection of aneuploidy in 4210 prenatal cases. JIA Chan-wei, WANG Shu-yu, MA Yan-min, LAN Yong-lian, YU Lan and ZHOU Li-ying. Chin Med J 2011;124(8): 1164-116.
dc.relation/*ref*/American College of Medical Genetics. (1993). Prenatal interphase fluorescence in situ hybrization (FlSH): policy statement. Am. J. Hum. Genet., 53:526-527.
dc.relation/*ref*/Naccache N., Jehee F., Bernal L.M., Gollop T.R. (1996). Amniocentese Precoce entre 12 e 15 semanas de gestação: Relato de 328 casos. Revista da Sociedade Brasileira de Medicina Fetal., 2:35-39.
dc.relation/*ref*/Ward B.E., Gersen S.L., Theve R., Wright M., Carelli M.P. Rapid prenatal diagnosis of cromosomal aneuploidies by flourescence in situ hybridization: clinical experience on 10000 specimens. ln: Pinkel D., Gray J.W. (eds). Clinical Applications of Fluorescence In Situ Hybridization, Chichester: John Wiley, in press. apudBryndorf T., Christensen B., Vad M., Pamer J., Brocks V., Philip J. (1997). Prenatal detection mof chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial. Prenat. D¡agn., 17(4):333-341.
dc.relation/*ref*/Carrera M., De la Iglesia C., Méndez B., Ribas l. (1996). Diagnóstico prenatal rápido de las principales aneuploídias fetales mediante hibridacáo in situ fluorescente: validación de la técnica. Prog. Diagn. Prenat., 8(5): 228-236.
dc.relation/*ref*/Thein A.T., Abdel-Fattah S.A., Kyle P.M,,SoothiIlP.W. (2000). An assessment of the use of interphase FlSH with chromosome specific probes as an alternative to cytogenetic in prenatal diagnosis. Prenat. Diagn., 20(4):275-280.
dc.relation/*ref*/Hook E.B., Cross P.K., Schreinemachers D.M. (1983). Chromosomal abnormality rates at amniocentesis and live-bom infants. JAMA., 249:2034-2038.
dc.relation/*ref*/Verlinsky Y., Ginsberg N., Chmura M., White M., Strom C., Kuliev A. (1998). Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FlSH. Prenat.Diagn., 18:390-392.
dc.relation/*ref*/Pettenati M.J., Berry M.N., Hart P.S., Rao P.N., Lantz P., Rosnes J. (1999).Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism.Prenat. Diagn., 19:25-28.
dc.relation/*ref*/Pergament E., Chen PX, Thangavelu M., Fiddler M. (2000). The clinical application of interphase FISH in prenatal diagnosis. Prenat. Diagn‘, 20(3):215-220.
dc.relation/*ref*/Divane A., Carter N.P., Spathas D.H., Ferguson-Smith M. A. (1944). Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescence in situ hybridization. Prenat. Diagn., 14:1061-1069.
dc.relation/*ref*/Cacheux V., Tachdjian G., Druart L., Oury J.F., Sérero 8., Blot P., Nessmann C. (1994). Evaluation of X, Y, 18 and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by flourescence in situ hybridization. Prenat.Diagn., 14:79-86.
dc.relation/*ref*/Bryndorf T., Christensen B., Vad M., Pamer J., Brocks V., Philip J. (1997). Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial. Prenat.Diagn., 17(4):333-341.
dc.relation/*ref*/Winsor E.J.T‘, Silver M.P., Theve R., Wright M., Ward B.E. (1996). Maternal cell contamination in uncultured amniotic fluid.Prenat. Diagn., 16:49-54.
dc.relation/*ref*/Benn P.A., Hsu L.Y.F. (1983). Maternal cell contamination of amniotic fluid cell cultures: results of a US nationwide survey. Am. J. Med. Genet., 15:297-305.
dc.relation/*ref*/Cuatrecasas E., Catalá V., Acevedo MIJ., Crespo M., Serés A. (1996). Contaminación en líquido amniótico detectada mediante citogenética e hibridación in situ. Prog.Diagn.Prenat, 8(5):244-251.
dc.rightsCopyright (c) 2011 NOVA Publicación en Ciencias Biomédicas
dc.rightshttp://creativecommons.org/licenses/by/4.0
dc.sourceNOVA Biomedical Sciences Journal; Vol. 9, Núm. 16 (2011); 129-137
dc.sourceNova; Vol. 9, Núm. 16 (2011); 129-137
dc.sourceNOVA Ciências Biomédicas Publicação; Vol. 9, Núm. 16 (2011); 129-137
dc.source2462-9448
dc.source1794-2470
dc.subjectCiencias Naturales,Ciencias Biológicas,Genética y Herencia
dc.subjectdiagnóstico prenatal; la amniocentesis temprana; la interfase FISH.
dc.subjectprenatal diagnosis; early amniocentesis; interphase FISH.
dc.titleFluorescence in Situ Hybridization (Fish) in Samples of Amniotic Fluid Obtained By Early Amniocentesis
dc.titleHibridación in Situ por Fluorescencia (Fish) en Muestras de Líquido Amniótico Obtenido por Amniocentesis Precoz
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typeinfo:eu-repo/article/published
dc.typeinfo:eu-repo/article/published
dc.typeinfo:eu-repo/article/published


Este ítem pertenece a la siguiente institución