Showing results (251-260 of 266) with videos related to
Sort By:
Pageof 27
American Journal of Human Genetics|April 1, 1989
Gene deletions in X-linked muscular dystrophyM Lindlöf, A Kiuru, H Kääriäinen, et al.American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.Neuromuscular Disorders : NMD|March 1, 1995
Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopyC Wallgren-Pettersson, B Jasani, G R Newman, et al.Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 1, 1992
Blood dolichol in lysosomal diseasesK Jokelainen, K S Salmela, K Humaloja, et al.Klinische Wochenschrift|May 24, 1991
Kidney biopsy findings in cyclosporine-treated patients with insulin-dependent diabetes mellitusM J Mihatsch, U Helmchen, P Casanova, et al.Pediatric Neurology|May 7, 2002
Phenotypic spectrum of Salla disease, a free sialic acid storage disorderTarja T Varho, Liisa E Alajoki, Kristiina M Posti, et al.Kidney International|September 6, 2000
Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patientsJ Patrakka, M Kestilä, J Wartiovaara, et al.Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.Pageof 27