Associated Papers
Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity.
Coste T et al.
Prenatal Diagnosis, 2025
39763161 (PubMed )
Supplement: supplement_1.docx
A case of venous thromboembolism caused by protein C deficiency due to a novel gene mutation.
Noiri JI et al.
Journal of Cardiology Cases, 2022
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