Associated Papers
A Genomic Sequencing Approach to Newborn Mass Screening and Its Opportunities.
Carli D et al.
Jama Network Open, 2025
41105405 (PubMed )
Supplement: jamanetwopen-e2538198-s001.xlsx › eTable_3
Clinical and Genetic Characterization of 51 Patients with Congenital Fibrinogen Disorders from China.
Cai Y et al.
Thrombosis and Haemostasis, 2025
Protein S Deficiency with Recurrent Thromboembolism after Splenectomy in a Patient with Hemoglobin H Disease.
Wu Y et al.
Mediterranean Journal of Hematology and Infectious Diseases, 2024
Distinctive regional-specific PROS1 mutation spectrum in Southern China.
Chan NCN et al.
Journal of Thrombosis and Thrombolysis, 2018
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