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Genomics|July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresisP Ritvaniemi, J Hyland, J Ignatius, et al.Neuropediatrics|May 1, 1987
Visual evoked potentials in high-risk infantsV K Häkkinen, J Ignatius, M Koskinen, et al.The Journal of Laboratory and Clinical Medicine|January 11, 2000
Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilitiesM J Nissinen, H Gylling, M Kaski, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 1, 1990
Neuron-specific expression of high-molecular-weight clathrin light chainD H Wong, M J Ignatius, G Parosky, et al.Journal of Biomedical Materials Research|April 29, 1998
Bioactive surface coatings for nanoscale instruments: effects on CNS neuronsM J Ignatius, N Sawhney, A Gupta, et al.Human Molecular Genetics|December 26, 2001
Dissecting a population genome for targeted screening of disease mutationsT Pastinen, M Perola, J Ignatius, et al.American Journal of Human Genetics|March 11, 2000
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2E Virolainen, M Wessman, I Hovatta, et al.Clinical Dysmorphology|April 2, 2004
Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated femalesMinna H Pöyhönen, Maarit M Peippo, Leena K Valanne, et al.Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.Pageof 9