Showing results (211-220 of 324) with videos related to
Sort By:
Pageof 33
Nature Genetics|August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethalityS Hirotsune, M W Fleck, M J Gambello, et al.American Journal of Medical Genetics|January 1, 1992
45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndromeM Grompe, N Rao, F F Elder, et al.Journal of Burn Care & Research : Official Publication of the American Burn Association|October 14, 2008
Risk factors for fires and burns in homebound, urban elderlyAmy R Ehrlich, Rebecca Y Bak, Paulette Wald-Cagan, et al.American Journal of Ophthalmology|June 15, 2011
Strabismus precipitated by monovisionZane F Pollard, Marc F Greenberg, Mark Bordenca, et al.Neurology|August 3, 1999
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.Journal of Medical Genetics|December 1, 1998
Two 22q telomere deletions serendipitously detected by FISHK S Precht, C M Lese, R P Spiro, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.Oncogene Research|August 1, 1987
Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21D J Tweardy, L A Cannizzaro, A P Palumbo, et al.Neurology|July 27, 2001
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX geneL Demelas, G Serra, M Conti, et al.Journal of Medical Genetics|March 19, 2002
Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qJ A Fantes, S K Mewborn, C M Lese, et al.Pageof 33