Screening and diagnosis of inherited platelet disorders
Author:
Affiliation:
1. Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada
2. Department of Medicine, McMaster University, Hamilton, Canada
Funder
Institute of Circulatory and Respiratory Health
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,General Biochemistry, Genetics and Molecular Biology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10408363.2022.2049199
Reference388 articles.
1. Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH
2. Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders
3. Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders
4. Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
5. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
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