Noninvasive Prenatal Diagnosis of Monogenic Disorders
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Elsevier
Reference52 articles.
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2. Implementing non-invasive prenatal diagnosis (NIPD) in a National Health Service Laboratory; from dominant to recessive disorders;Drury;Adv Exp Med Biol,2016
3. Analysis of cell-free fetal DNA for non-invasive prenatal diagnosis in a family with neonatal diabetes;De Franco;Diabet Med,2017
4. Droplet digital PCR combined with minisequencing, a new approach to analyse fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia;Orhant;Prenat Diagn,2016
5. Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach;Chitty;Prenat Diagn,2015
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1. Integration of targeted sequencing and pseudo-tetraploid genotyping into clinically assisted decision support for β-thalassemia invasive prenatal diagnosis;PLOS ONE;2023-04-04
2. Noninvasive detection of fetal genetic variations through polymorphic site sequencing of maternal plasma DNA;The Journal of Gene Medicine;2021-12-14
3. The Impact of Cell-Free DNA Analysis on the Management of Retinoblastoma;Cancers;2021-03-29
4. Noninvasive Detection of Fetal Genetic Variations through Polymorphic Sites Sequencing of Maternal Plasma DNA;2021-01-29
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