Genome-Wide Noninvasive Prenatal Diagnosis of De Novo Mutations
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-0716-1103-6_12
Reference36 articles.
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3. Hayward J, Chitty LS (2018) Beyond screening for chromosomal abnormalities: advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing. Semin Fetal Neonatal Med 23:94–101. https://doi.org/10.1016/j.siny.2017.12.002
4. Akolekar R, Beta J, Picciarelli G et al (2015) Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis. Ultrasound Obstet Gynecol 45:16–26. https://doi.org/10.1002/uog.14636
5. Tabor A, Alfirevic Z (2010) Update on procedure-related risks for prenatal diagnosis techniques. Fetal Diagn Ther 27:1–7. https://doi.org/10.1159/000271995
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