Utility of whole-genome sequencing for underlying monogenic disorders in routine newborn screening: Perspectives

China National GeneBank DataBase 2026 Open access

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Authors: 张国洪
DOI: 10.26036/cnp0005396
Cited by: 0

Abstract

Utility of whole-genome sequencing for underlying monogenic disorders in routine newborn screening: Perspectives on Qingdao region-wide newborn screening project

Fields of Study & Subjects

Genomics and Rare Diseases Metabolism and Genetic Disorders Prenatal Screening and Diagnostics

Publication details

Journal / source
China National GeneBank DataBase
Publication date
1 January 2026
Language
EN