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Genomics|November 26, 1998
Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24S J Mansour, J A Herbrick, S W Scherer, et al.Genomics|March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14qR F Wintle, T G Nygaard, J A Herbrick, et al.Biochemical and Biophysical Research Communications|July 2, 1998
Structural characterization and mapping of the normal epithelial cell-specific 1 geneL Luo, J A Herbrick, S W Scherer, et al.Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.Genomics|January 25, 2000
Chromosomal localization of phospholipase A2 activating protein, an Ets2 target gene, to 9p21B G Beatty, S Qi, M Pienkowska, et al.Human Molecular Genetics|June 9, 1998
Molecular analysis of the PDS gene in Pendred syndromeB Coyle, W Reardon, J A Herbrick, et al.Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.Pageof 2