Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation

Congenital malformations diagnosed by ultrasound screening complicate 3–5% of pregnancies and many of these have an underlying genetic cause. Approximately 40% of prenatally diagnosed fetal malformations are associated with aneuploidy or copy number variants, detected by conventional karyotyping, QF...

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Detalles Bibliográficos
Autores principales: Emms, Alexandra, Castleman, James, Allen, Stephanie, Williams, Denise, Kinning, Esther, Kilby, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498826/
https://www.ncbi.nlm.nih.gov/pubmed/36140685
http://dx.doi.org/10.3390/genes13091517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498826/
https://www.ncbi.nlm.nih.gov/pubmed/36140685
http://dx.doi.org/10.3390/genes13091517

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