Cargando…
Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool
Introduction: Prenatal ultrasound (US) anomalies are detected in around 5%–10% of pregnancies. In prenatal diagnosis, exome sequencing (ES) diagnostic yield ranges from 6% to 80% depending on the inclusion criteria. We describe the first French national multicenter pilot study aiming to implement ES...
Ejemplares similares
-
Interest of exome sequencing trio‐like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases
por: Tran Mau‐Them, Frederic, et al.
Publicado: (2021) -
The diagnostic rate of inherited metabolic disorders by exome sequencing in a cohort of 547 individuals with developmental disorders
por: Delanne, Julian, et al.
Publicado: (2021) -
Combining globally search for a regular expression and print matching lines with bibliographic monitoring of genomic database improves diagnosis
por: Tran Mau-Them, Frédéric, et al.
Publicado: (2023) -
Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination
por: Trimouille, Aurélien, et al.
Publicado: (2020) -
Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing
por: Cospain, Auriane, et al.
Publicado: (2020)