Prenatal diagnosis of fetal chromosomal abnormalities: report of an 18-year experience in a Brazilian public hospital
Author:
Affiliation:
1. Hospital de Clínicas de Porto Alegre, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v31n4/04.pdf
Reference21 articles.
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2. Prenatal cytogenetic diagnosis: Gone FISHing, BAC soon;Bui TH;Ultrasound Obstet Gynecol,2007
3. Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analysis;Caron L;Am J Med Genet,1999
4. Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings;Carothers AD;Genet Epidemiol,1999
5. First-trimester nuchal translucency measurement and echo-cardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18;Cheng PJ;Prenat Diagn,2003
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2. Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations;European Journal of Human Genetics;2022-01-01
3. Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women;Scientific Reports;2021-09-30
4. The most relevant chromosomal abnormalities in the north of Rio Grande do Sul, Brazil: 26 years of cytogenetic analysis;Annals of Human Biology;2019-01-02
5. Prevalência das malformações congênitas identificadas em fetos com trissomia dos cromossomos 13, 18 e 21;Revista Brasileira de Ginecologia e Obstetrícia;2015-07
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