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UnknownIdentification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.
Not available
S-EPMC5594472 | biostudies-literature
UnknownSomatic mosaicism in hemophilia A: a fairly common event.
Not available
S-EPMC1226050 | biostudies-literature
UnknownHemophilia B: molecular pathogenesis and mutation analysis.
Not available
S-EPMC4496316 | biostudies-literature
UnknownIn silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion.
Not available
S-EPMC5960579 | biostudies-literature
Unknownvon Willebrand disease.
Not available
S-EPMC3832952 | biostudies-literature
UnknownIdentification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.
Not available
S-EPMC4213552 | biostudies-literature
UnknownIdentification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).
Not available
S-EPMC2384129 | biostudies-literature
UnknownAssessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.
Not available
S-EPMC4220540 | biostudies-literature
UnknownGenotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
Not available
S-EPMC8361454 | biostudies-literature
UnknownPhenotypic and Genotypic Signatures of VWF Exon 18 in Eastern Saudi Patients Previously Diagnosed with Type 1 von Willebrand Disease.
Not available
S-EPMC9170233 | biostudies-literature
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