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The diagnostic trajectory of infants and children with clinical features of genetic disease

The diagnostic trajectory of infants and children with clinical features of genetic disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_eb3713872ddf488086a7b015eca24269

The diagnostic trajectory of infants and children with clinical features of genetic disease

About this item

Full title

The diagnostic trajectory of infants and children with clinical features of genetic disease

Publisher

London: Nature Publishing Group UK

Journal title

Npj genomic medicine, 2021-11, Vol.6 (1), p.98-98, Article 98

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

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 genetic disease in healthcare claims from Optum’s de-identified...

Alternative Titles

Full title

The diagnostic trajectory of infants and children with clinical features of genetic disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_eb3713872ddf488086a7b015eca24269

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_eb3713872ddf488086a7b015eca24269

Other Identifiers

ISSN

2056-7944

E-ISSN

2056-7944

DOI

10.1038/s41525-021-00260-2

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