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Clinical Chemistry|January 1, 1997
Development of reverse dot-blot system for screening of mitochondrial DNA mutations associated with Leber hereditary optic atrophyE Schollen, P Vandenberk, J J Cassiman, et al.The American Journal of Physiology|July 1, 1990
Effects of substance P on [Ca2+]i and force in intact guinea pig ileal smooth muscleG Matthijs, B Himpens, T L Peeters, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.Acta Clinica Belgica|August 3, 2002
Noniatrogenic haemochromatosis in congenital dyserythropoietic anaemia type II is not related to C282Y and H63D mutations in the HFE gene: report on two brothersW Van Steenbergen, G Matthijs, T Roskams, et al.Biochimica Et Biophysica Acta|November 26, 1999
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)H Carchon, E Van Schaftingen, G Matthijs, et al.European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.Journal of Inherited Metabolic Disease|October 25, 2008
On the nomenclature of congenital disorders of glycosylation (CDG)J Jaeken, T Hennet, H H Freeze, et al.Regulatory Peptides|November 1, 1986
Comparison of the biological activity of canine and porcine motilin in rabbitT L Peeters, V Bormans, G Matthijs, et al.DNA and Cell Biology|June 1, 1996
Characterization of a helicase-like transcription factor involved in the expression of the human plasminogen activator inhibitor-1 geneH Ding, K Descheemaeker, P Marynen, et al.Cytogenetic and Genome Research|March 9, 2004
A physical map of the chromosome 12 centromereJ R Vermeesch, H Duhamel, P Raeymaekers, et al.Pageof 28