Publicación:
Indicaciones de estudio genético invasivo en una población seleccionada: Agosto de 2005 a diciembre de 2007

Vista sencilla de ítem
dc.contributor.authorAlcedo Ramírez, Alezander D.spa
dc.contributor.authorSerrano Serrano, Claudiaspa
dc.contributor.authorRojas, José Luiisspa
dc.contributor.authorMolina Giraldo, Saulospa
dc.contributor.authorAcuña Osorio, Edgar Marianospa
dc.contributor.authorFranco, Alejandrospa
dc.contributor.authorGalvis, Pablospa
dc.contributor.authorArévalo, Ingridspa
dc.date.accessioned2009-06-01 00:00:00
dc.date.accessioned2022-02-21T20:37:27Z
dc.date.available2009-06-01 00:00:00
dc.date.available2022-02-21T20:37:27Z
dc.date.issued2009-06-01
dc.format.mimetypeapplication/pdfspa
dc.identifier.doi10.31260/RepertMedCir.v18.n2.2009.538
dc.identifier.eissn2462-991X
dc.identifier.issn0121-7372
dc.identifier.urihttps://repositorio.fucsalud.edu.co/handle/001/2432
dc.identifier.urlhttps://doi.org/10.31260/RepertMedCir.v18.n2.2009.538
dc.language.isospaspa
dc.publisherFundación Universitaria de Ciencias de la Saludspa
dc.relation.bitstreamhttps://revistas.fucsalud.edu.co/index.php/repertorio/article/download/538/578
dc.relation.citationeditionNúm. 2 , Año 2009 : Abril - Juniospa
dc.relation.citationendpage105
dc.relation.citationissue2spa
dc.relation.citationstartpage97
dc.relation.citationvolume18spa
dc.relation.ispartofjournalRevista Repertorio de Medicina y Cirugíaspa
dc.relation.referencesAlfirevic Z, Sundberg K, Brigham S. Amniocentesis and chorionic villus sampling for prenatal diagnosis. Cochrane Database Syst Rev. 2003; (3):CD003252.spa
dc.relation.referencesAmerican College of Obstetricians and Gynecologists. ACOG Practice Bulletin No. 88. Invasive Prenatal testing for aneuploidy. Obstet Gynecol. 2007; 110 (6): 1459-67. 3. Cuckle HS, Wald NJ. Principles of screening. In: Wald NJ, editor. Antenatal and neonatal screening. Oxford: Oxford University Press; 2008. p 1–22.spa
dc.relation.referencesGardner RJ, Sutherland GR. Chromosome abnormalities and genetic counseling. 3rd ed. New York : Oxford University Press; 2004.spa
dc.relation.referencesMilunsky A, Milunsky JM. Genetic counseling: preconception, prenatal, and perinatal. In: Milunsky A, editor. Genetic disorders and the fetus: diagnosis, prevention, and treatment. 5th ed. Baltimore (MD): Johns Hopkins University Press; 2004. p. 1–65.spa
dc.relation.referencesReddy UM, Wapner RJ. Comparison of first and second trimester aneuploidy risk assessment. Clin Obstet Gynecol. 2007; 50(2): 442-53.spa
dc.relation.referencesEgan JF, Benn PA, Zelop CM, et al. Down syndrome births in the United States from 1989 to 2001. Am J Obstet Gynecol. 2004; 191 (3):1044–48.spa
dc.relation.referencesNicolaides KH. Screening for chromosomal defects. Ultrasound Obstet Gynecol. 2003; 21 (4): 313-21.spa
dc.relation.referencesVerdin SM, Whitlow BJ, Lazanakis M, Kadir RA, Chatzipapas I, Economides DL. Ultrasonographic markers for chromosomal abnormalities in women with negative nuchal translucency and second trimester maternal serum biochemistry. Ultrasound Obstet Gynecol. 2000; 16 (5): 402-6.spa
dc.relation.referencesShipp TD, Benacerraf BR. Second trimester ultrasound screening for chromosomal abnormalities. Prenat Diagn. 2002; 22 (4): 296–307.spa
dc.relation.referencesSimpson JL. Prenatal cytogenetic screening. Ultrasound Obstet Gynecol. 1995; 5 (1): 3-5spa
dc.relation.referencesSaller DN, Canick JA. Current methods of prenatal screening for Down syndrome and other fetal abnormalities. Clin Obstet Gynecol. 2008; 51(1): 24-36spa
dc.relation.referencesResta RG. Changing demographics of advanced maternal age (AMA) and the impact on the predicted incidence of Down syndrome in the United States: implications for prenatal screening and genetic counseling. Am J Med Genet. 2005; 133A (1):31-6.spa
dc.relation.referencesChorionic villus sampling and amniocentesis: recommendations for prenatal counseling. Centers for Disease Control and Prevention. MMWR Recomm Rep. 1995; 44 (RR-9):1–12.spa
dc.relation.referencesSeeds W. Diagnostic mid trimester amniocentesis: how safe?. Am J Obstet Gynecol. 2004; 191(2): 607–15.spa
dc.relation.referencesCaughey AB, Hopkins LM, Norton ME. Chorionic villus sampling compared with amniocentesis and the difference in the rate of pregnancy loss. Obstet Gynecol. 2006; 108 (3 pt 1):612–16.spa
dc.relation.referencesAmerican College of Obstetricians and Gynecologists. ACOG Practice Bulletin No. 77. Screening for fetal chromosomal abnormalities. Obstet Gynecol. 2007; 109 (1): 217–28.spa
dc.relation.referencesNicolaides KH, Spencer K, Avgidou K, Faiola S, Falcon O. Multicenter study of first-trimester screening for trisomy 21 in 75 821 pregnancies: results and estimation of the potential impact of individual risk-orientated twostage first-trimester screening. Ultrasound Obstet Gynecol. 2005; 25 (3): 221–26.spa
dc.relation.referencesWald NJ, Rodeck C, Hackshaw AK, Walters J, Chitty L, Mackinson AM. First and second trimester antenatal screening for Down’s syndrome: the results of the serum, urine and ultrasound screening study (SURUSS). Health Technol Assess. 2003; 7 (11): 1-77.spa
dc.relation.referencesBorgida AF, Mills AA, Feldman DM, Rodis JF, Egan JF. Outcome of pregnancies complicated by ruptured membranes after genetic amniocentesis. Am J Obstet Gynecol. 2000; 183(4): 937–9.spa
dc.relation.referencesCicero S, Curcio P, Papageorghiou A, Sonek J, Nicolaides KH. Absence of nasal bone in fetuseswith trisomy 21 at 11–14 weeks of gestation: an observational study. Lancet. 2001; 358 (9294):1665–67.spa
dc.relation.referencesMatias A, Gomes C, Flack N, Montenegro N, Nicolaides KH. Screening for chromosomal abnormalities at 11–14 weeks: the role of ductus venosus blood flow. Ultrasound Obstet Gynecol.1998; 12 (6): 380–84.spa
dc.relation.referencesHuggon IC, DeFigueiredo DB, Allan LD. Tricuspid regurgitation in the diagnosis of chromosomal anomalies in the fetus at 11–14 weeks of gestation. Heart. 2003; 89 (9): 1071–73.spa
dc.relation.referencesTabor A, Philip J, Madsen M, et al. Randomised controlled trial of genetic amniocentesis in 4606 lowrisk women. Lancet. 1986; 1 (8493):1287–93.spa
dc.relation.referencesRalston SJ, Craigo SD. Ultrasound-guided procedures for prenatal diagnosis and therapy. Obstet Gynecol Clin N Am. 2004; 31 (1) 101–23.spa
dc.rightsFundación Universitaria de Ciencias de la Salud FUCS - 0spa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.rights.coarhttp://purl.org/coar/access_right/c_abf2spa
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.sourcehttps://revistas.fucsalud.edu.co/index.php/repertorio/article/view/538spa
dc.subjecttranslucencia nucalspa
dc.subjectcariotipospa
dc.subjectsíndromes genéticosspa
dc.subjectanomalías estructuralesspa
dc.subjectscreening prenatalspa
dc.subjectsíndrome de Downspa
dc.subjectNuchal translucencyeng
dc.subjectkaryotypeeng
dc.subjectgenetic syndromeseng
dc.subjectstructural anomalieseng
dc.subjectprenatal screeningeng
dc.subjectDown syndromeeng
dc.titleIndicaciones de estudio genético invasivo en una población seleccionada: Agosto de 2005 a diciembre de 2007spa
dc.title.translatedIndications of invasive genetic study in a selected population: August 2005 to December 2007eng
dc.typeArtículo de revistaspa
dc.typeJournal articleeng
dc.type.coarhttp://purl.org/coar/resource_type/c_6501spa
dc.type.coarversionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.type.contentTextspa
dc.type.driverinfo:eu-repo/semantics/articlespa
dc.type.versioninfo:eu-repo/semantics/publishedVersionspa
dspace.entity.typePublication

Archivos

Colecciones

BA. Revista Repertorio