Showing results (71-80 of 102) with videos related to
Sort By:
Pageof 11
Vox Sanguinis|January 1, 1986
Proposal for the nomenclature of human plasminogen (PLG) polymorphismU Skoda, J Bertrams, D Dykes, et al.Human Mutation|January 1, 1996
Allele-specific measurement of low-density lipoprotein receptor transcript levelsL G Jensen, H K Jensen, F Heath, et al.The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasiansL Hansen, S Urioste, H V Petersen, et al.Proceedings of the National Academy of Sciences of the United States of America|June 24, 1997
Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinomaK Helin, K Holm, A Niebuhr, et al.Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|February 5, 2009
Polymorphic drug metabolizing CYP-enzymes--a pathogenic factor in oral lichen planus?C Kragelund, C Hansen, J Reibel, et al.European Journal of Neurology|May 20, 2014
Risk of cancer in relatives of patients with myotonic dystrophy: a population-based cohort studyM Lund, L J Diaz, S Gørtz, et al.Journal of Medical Genetics|April 5, 2005
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)K W Kjaer, L Hansen, G C Schwabe, et al.Clinical Genetics|May 1, 1986
Linkage between the loci for cystic fibrosis and paraoxonaseK Schmiegelow, H Eiberg, L C Tsui, et al.The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
The effect of two frequent amino acid variants of the hepatocyte nuclear factor-1alpha gene on estimates of the pancreatic beta-cell function in Caucasian glucose-tolerant first-degree relatives of type 2 diabetic patientsS A Urhammer, A M Møller, B Nyholm, et al.Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.Pageof 11