Editorial: Improving medical diagnosis in rare diseases. | Front Genet;13: 974129, 2022. | MEDLINE

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Editorial: Improving medical diagnosis in rare diseases.

Linhares, Natália Duarte; Gorman, Kathleen M; Brusco, Alfredo.

Affiliation

Linhares ND; Genuity Science, Dublin, Ireland.
Gorman KM; Department of Neurology and Clinical Neurophysiology, Children's Health Ireland at Temple St., Dublin, Ireland.
Brusco A; School of Medicine and Medical Science, University College Dublin, Dublin, Ireland.

Front Genet ; 13: 974129, 2022.

Article in En | MEDLINE | ID: mdl-36147485

Key words

Rare disease (RD); diagnosis; next-generation sequencing (NGS); whole-exome sequencing (WES); whole-genome sequencing (WGS)

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Ireland Country of publication: Switzerland

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Ireland Country of publication: Switzerland