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Genomics|December 15, 1996
Characterization of human DSPG3, a small dermatan sulfate proteoglycanM Deere, J Johnson, S Garza, et al.Schizophrenia Research|August 7, 2012
Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: a pilot studyZ Kikinis, T Asami, S Bouix, et al.Genomics|September 1, 1993
Characterization of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISHK T Montgomery, J M LeBlanc, P Tsai, et al.American Journal of Human Genetics|November 1, 1995
Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12E C Engle, I Marondel, W A Houtman, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1997
Retinal pigment epithelium abnormalities in mice with adenomatous polyposis coli gene disruptionD M Marcus, A K Rustgi, D Defoe, et al.Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome regionA Puech, B Saint-Jore, S Merscher, et al.Genes & Development|October 23, 1997
K-ras is an essential gene in the mouse with partial functional overlap with N-rasL Johnson, D Greenbaum, K Cichowski, et al.Genes, Chromosomes & Cancer|June 22, 2000
Genetic analysis of the APAF1 gene in male germ cell tumorsS Bala, H Oliver, B Renault, et al.Genes & Development|May 16, 2000
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female miceB Kneitz, P E Cohen, E Avdievich, et al.The Journal of Cell Biology|January 7, 1998
Growth and muscle defects in mice lacking adult myosin heavy chain genesL J Acakpo-Satchivi, W Edelmann, C Sartorius, et al.Pageof 12