Prenatal diagnosis of genetic disorders
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference8 articles.
1. Cell-free fetal DNA: the new tool in fetal medicine;Everett;Ultrasound Obstet Gynecol,2014
2. Recommendations for the use of chromosome microarray in pregnancy;Gardiner,2015
3. Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol;Hill;BMC Pregnancy Childbirth,2014
4. Use of prenatal chromosomal microarray: prospective cohort study and systemic review and meta-analysis;Hillman;Ultrasound Obstet Gynecol,2013
5. How to use microarray comparative genomic hybridisation to investigate developmental disorders;Kharbanda;Arch Dis Child Educ Pract Ed,2015
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1. De novo variants of dominant monogenic disorders in Vietnam detected by a noninvasive prenatal test: a case series;Personalized Medicine;2023-11-08
2. scRNA-Seq of Cultured Human Amniotic Fluid from Fetuses with Spina Bifida Reveals the Origin and Heterogeneity of the Cellular Content;Cells;2023-06-07
3. Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy;Molecular Genetics & Genomic Medicine;2020-04-12
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