Laboratory Guidelines for Detection, Interpretation, and Reporting of Maternal Cell Contamination in Prenatal Analyses
Author:
Publisher
Elsevier BV
Subject
Molecular Medicine,Pathology and Forensic Medicine
Reference8 articles.
1. Practice of prenatal diagnosis in the UK;Macdonald;Clinical Risk,2008
2. Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping;Stojilkovic-Mikic;Prenat Diagn,2005
3. Maternal cell contamination in uncultured amniotic fluid;Winsor;Prenat Diagn,1996
4. Early amniocentesis versus chorionic villus sampling for fetal karyotyping;Saura;Lancet,1994
5. Testing for maternal cell contamination in prenatal samples: a comprehensive survey of current diagnostic practices in 35 molecular diagnostic laboratories;Schrijver;J Mol Diagn,2007
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2. Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis;Journal of Medical Genetics;2024-06-04
3. Maternal cell contamination in postnatal umbilical cord blood samples implies a low risk for genetic misdiagnoses;Prenatal Diagnosis;2024-05-23
4. Applications of next generation sequencing in the screening and diagnosis of thalassemia: A mini-review;Frontiers in Pediatrics;2022-09-29
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