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Proceedings of the National Academy of Sciences of the United States of America|February 3, 1999
Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin geneD A Stephan, E Gillanders, D Vanderveen, et al.Genomics|April 25, 2001
Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locusR Sood, T I Bonner, I Makalowska, et al.Biochimica Et Biophysica Acta|April 13, 2000
The human RGL (RalGDS-like) gene: cloning, expression analysis and genomic organizationR Sood, I Makalowska, J D Carpten, et al.Neurology|September 7, 2007
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5C Wider, S Melquist, M Hauf, et al.Molecular Psychiatry|February 28, 2008
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12M Romanos, C Freitag, C Jacob, et al.Genomics|March 10, 2000
A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) regionJ D Carpten, I Makalowska, C M Robbins, et al.Pageof 3