Associated Papers
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.4
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
Rectal cancer sub-clones respond differentially to neoadjuvant therapy.
Frydrych LM et al.
Neoplasia (new York, N.y.), 2019
31521947 (PubMed )
Supplement: mmc2.xlsx › sheet1
[Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].
Chen T et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2018
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.
Kulkarni BP et al.
Plos One, 2014
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran.
Karimi M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2012
Select a paper to view details