Prenatal Diagnosis of Congenital Human Cytomegalovirus Infection in Amniotic Fluid by Nucleic Acid Sequence-Based Amplification Assay
Author:
Affiliation:
1. Servizio di Virologia, Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, 27100 Pavia, Italy
2. Free University of Amsterdam, Amsterdam, The Netherlands
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.41.4.1772-1774.2003
Reference17 articles.
1. Bodéus, M., C. Hubinont, P. Bernard, A. Bouckaert, K. Thomas, and P. Goubau. 1999. Prenatal diagnosis of human cytomegalovirus by culture and polymerase chain reaction: 98 pregnancies leading to congenital infection. Prenatal Diagn.19:314-317.
2. Donner, C., C. Liesnard, F. Brancart, and F. Rodesch. 1994. Accuracy of amniotic fluid testing before 21 weeks' gestation in prenatal diagnosis of congenital cytomegalovirus infection. Prenatal Diagn.14:1055-1059.
3. Donner, C., C. Liesnard, J. Content, A. Busine, J. Aderca, and F. Rodesch. 1993. Prenatal diagnosis of 52 pregnancies at risk for congenital cytomegalovirus infection. Obstet. Gynecol.82:481-486.
4. Enders, G., U. Bäder, L. Lindemann, G. Schalasta, and A. Daiminger. 2001. Prenatal diagnosis of congenital cytomegalovirus infection in 189 pregnancies with known outcome. Prenatal Diagn.21:362-377.
5. Real-Time PCR Quantification of Human Cytomegalovirus DNA in Amniotic Fluid Samples from Mothers with Primary Infection
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