Pages that link to "Q45862187"

The following pages link to Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients (Q45862187):

Displaying 34 items.

• von Willebrand disease: clinical and laboratory lessons learned from the large von Willebrand disease studies (Q26863636) (← links)
• Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding (Q33369028) (← links)
• Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor (Q33998293) (← links)
• von Willebrand Disease. (Q34546675) (← links)
• Clinical utility gene card for: von Willebrand disease (Q34873778) (← links)
• Haematology research in India: past, present and future (Q35106402) (← links)
• Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients (Q35133215) (← links)
• Clinical diagnosis of von Willebrand disease (Q35915740) (← links)
• Genetic diagnosis of haemophilia and other inherited bleeding disorders. (Q36473065) (← links)
• Alloantibodies in von Willebrand disease (Q37065692) (← links)
• Pharmacokinetics and safety of a novel recombinant human von Willebrand factor manufactured with a plasma-free method: a prospective clinical trial (Q37077021) (← links)
• von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). (Q37100261) (← links)
• The molecular genetics of von Willebrand disease (Q37193881) (← links)
• p.P2063S: a neutral VWF variant masquerading as a mutation (Q37325651) (← links)
• The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles (Q37524379) (← links)
• Laboratory testing for von Willebrand disease: toward a mechanism-based classification (Q37576572) (← links)
• Translational medicine advances in von Willebrand disease (Q37602563) (← links)
• von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein (Q37903943) (← links)
• Hemostasis research in India: past, present, and future (Q39022458) (← links)
• Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations (Q39388978) (← links)
• The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients (Q41919816) (← links)
• Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay (Q42938324) (← links)
• Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study (Q45857734) (← links)
• Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease (Q45875800) (← links)
• Gene conversions are a common cause of von Willebrand disease (Q46662869) (← links)
• An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees (Q46892241) (← links)
• A 12.3 kb Duplication Within the VWF Gene in Pigs Affected by Von Willebrand Disease Type 3. (Q47326585) (← links)
• Novel insights into the clinical phenotype and pathophysiology underlying low VWF levels (Q47793791) (← links)
• Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort (Q50965737) (← links)
• [Mutation analysis of VWF gene in two patients with von Willebrand disease by target sequence capture and high-throughput sequencing technology]. (Q52644655) (← links)
• A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3 (Q58492974) (← links)
• The study of the effect of splicing mutations in von Willebrand factor using RNA isolated from patients’ platelets and leukocytes (Q83249216) (← links)
• [Research progress of alloantibodies against von Willebrand factor] (Q85270703) (← links)
• Cryptic non-canonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor (Q92002036) (← links)