Open standard CMO for parametric modelling based on semantic web

Translational research in genomics of Alzheimer's disease: A review of current practice and future perspectives

Phenotypic and molecular characterization of Bruck syndrome (Osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2

Fundus reflectance: Historical and present ideas

Genetic analysis of indicators of cholesterol synthesis and absorption: Lathosterol and phytosterols in Dutch twins and their parents

An amino acid polymorphism in histidine-rich glycoprotein (HRG) explains 59% of the variance in plasma HRG levels

Identification and genetic analysis of a common molecular variant of histidine-rich glycoprotein with a difference of 2KD in apparent molecular weight

Triglyceride-rich lipoproteins of subjects heterozygous for apolipoprotein E2(Lys146 → Gln) are inefficiently converted to cholesterol-rich lipoproteins

a2-Antiplasmin Enschede: Dysfunctional alpha 2-antiplasmin molecule associated with an autosomal recessive hemorrhagic disorder

A familial hemorrhagic diathesis in a Dutch family: An inherited deficiency of ??2-antiplasmin