The diagnostic trajectory of infants and children with clinical features of genetic disease
Abstract We characterized US pediatric patients with clinical indicators of genetic diseases, focusing on the burden of disease, utilization of genetic testing, and cost of care. Curated lists of diagnosis, procedure, and billing codes were used to identify patients with clinical indicators of genet...
Guardado en:
Autores principales: | Brock E. Schroeder, Nina Gonzaludo, Katie Everson, Kyi-Sin Than, Jeff Sullivan, Ryan J. Taft, John W. Belmont |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/eb3713872ddf488086a7b015eca24269 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.
por: Chenxing Liu, et al.
Publicado: (2021) -
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.
por: Gary W Beecham, et al.
Publicado: (2014) -
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
por: Nathaly M. Sweeney, et al.
Publicado: (2021) -
The Prevalence of Clinical Features in Patients with Aarskog–Scott Syndrome and Assessment of Genotype-Phenotype Correlation: A Systematic Review
por: Victor Zanetti Drumond, et al.
Publicado: (2021) -
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
por: Nathaly M. Sweeney, et al.
Publicado: (2021)