Associated Papers
Molecular and clinical profile of rare bleeding disorders: A single-center retrospective study.
Moghadam AA et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2024
Factor VII deficiency in China: Phenotype, genotype and current status of management.
Qu C et al.
British Journal of Haematology, 2023
Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency.
Zhang X et al.
Journal of Clinical Laboratory Analysis, 2021
Molecular classification of blood and bleeding disorder genes.
Baz B et al.
Npj Genomic Medicine, 2021
34272389 (PubMed )
Supplement: 41525_2021_228_MOESM1_ESM.pdf
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.
Karimi M et al.
Haematologica, 2008
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