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Human Genetics|August 1, 1994
Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy geneF Rininsland, J ReissHuman Molecular Genetics|February 1, 1994
An explanation for the constitutive exon 9 cassette splicing of the DMD geneJ Reiss, F RininslandMolecular and Cellular Probes|February 1, 1992
Simple non-radioactive detection of the CFTR mutation N1303K by artificial creation of a restriction siteJ Bal, F Rininsland, L Osborne, et al.Human Genetics|September 1, 1994
Skipping of multiple CFTR exons is not a result of single exon omissionsA Rickers, F Rininsland, L Osborne, et al.Human Genetics|January 1, 1992
Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patientsJ Plieth, F Rininsland, M Schlösser, et al.Proceedings of the National Academy of Sciences of the United States of America|July 9, 1996
Antisense RNA to the type I insulin-like growth factor receptor suppresses tumor growth and prevents invasion by rat prostate cancer cells in vivoP Burfeind, C L Chernicky, F Rininsland, et al.American Journal of Human Genetics|December 1, 1991
A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ Zielenski, D Markiewicz, F Rininsland, et al.Human Genetics|November 1, 1992
A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysisJ Reiss, U Lenz, F Rininsland, et al.Human Genetics|September 1, 1992
Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophyS Niemann-Seyde, R Slomski, F Rininsland, et al.Journal of Medical Genetics|September 1, 1992
Identification of a new DMD gene deletion by ectopic transcript analysisF Rininsland, A Hahn, S Niemann-Seyde, et al.Pageof 2