Challenges in the clinical understanding of genetic testing in birth defects and pediatric diseases

Advances in prenatal/neonatal genetic screening practices and next generation sequencing (NGS) technologies have made the detection of molecular causes of pediatric diseases increasingly more affordable, accessible, and rapid in return of results. In the past, families searching for answers often re...

Descripción completa

Detalles Bibliográficos
Autores principales: Findley, Tina O., Parchem, Jacqueline G., Ramdaney, Aarti, Morton, Sarah U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248941/
https://www.ncbi.nlm.nih.gov/pubmed/37305724
http://dx.doi.org/10.21037/tp-23-54

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248941/
https://www.ncbi.nlm.nih.gov/pubmed/37305724
http://dx.doi.org/10.21037/tp-23-54

Ejemplares similares