An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders

Chung, W. K., Kanne, S. M., & Hu, Z. (2024). An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders. International Journal of Neonatal Screening, 10(2), 33. https://doi.org/10.3390/ijns10020033
Authors:
Wendy K. Chung
Stephen M. Kanne
Zhanzhi Hu
Affiliated Authors:
Zhanzhi Hu
Columbia Affiliation:
Subjects:
Standards and Guidelines for Genetic Variant Interpretation (OpenAlex Topic)
Molecular Basis of Rett Syndrome and Related Disorders (OpenAlex Topic)
Autism Spectrum Disorders (OpenAlex Topic)
Author Keywords:
early intervention program (eip)
genome sequencing (gs)
genomic uniform screening against rare diseases in all newborns (guardian)
neurodevelopmental disorder (ndd)
newborn screening (nbs)
variants of unknown significance (vus)
elink
Publication Type:
Article
Unique ID:
10.3390/ijns10020033
PMID:
38651398
DOI:
10.3390/ijns10020033
Journal:
International Journal of Neonatal Screening
Publication Date:
Data Source:
OpenAlex
Source Link:
View OpenAlex Record
View PubMed Record

Record Created: