Showing results (21-30 of 41) with videos related to
Sort By:
Pageof 5
American Journal of Human Genetics|December 5, 1998
Multiple molecular mechanisms underlying subdiagnostic variants of Marfan syndromeR A Montgomery, M T Geraghty, E Bull, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Detecting patterns of protein distribution and gene expression in silicoM T Geraghty, D Bassett, J C Morrell, et al.Journal of Inherited Metabolic Disease|December 22, 1999
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variationS L White, S Shanske, J J McGill, et al.Genomics|May 1, 1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YACM T Geraghty, L C Brody, L S Martin, et al.American Journal of Medical Genetics|September 5, 1997
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden diseaseE M Arch, B K Goodman, R A Van Wesep, et al.Human Molecular Genetics|March 21, 1998
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsL T Braiterman, S Zheng, P A Watkins, et al.Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.American Journal of Human Genetics|April 25, 2000
Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemiaK A Sacksteder, B J Biery, J C Morrell, et al.Human Molecular Genetics|May 1, 1994
Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpointB de Leeuw, M Balemans, D O Weghuis, et al.Human Molecular Genetics|August 13, 1998
Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemiaM T Geraghty, D Vaughn, A J Nicholson, et al.Pageof 5