Showing results (41-50 of 109) with videos related to
Sort By:
Pageof 11
Journal of Pediatric Gastroenterology and Nutrition|December 14, 2019
Direct Health Care Costs, Health Services Utilization, and Outcomes of Biliary Atresia: A Population-based Cohort StudyShabnaz Siddiq, Carolina Jimenez-Rivera, M Ellen Kuenzig, 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.Plos One|October 3, 2013
Population expansion and genetic structure in Carcharhinus brevipinna in the southern Indo-PacificPascal T Geraghty, Jane E Williamson, William G Macbeth, 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.Journal of Fish Biology|August 8, 2015
Age and growth of the tiger shark Galeocerdo cuvier off the east coast of AustraliaB J Holmes, V M Peddemors, A N Gutteridge, et al.JIMD Reports|July 7, 2014
Analysis of methylcitrate in dried blood spots by liquid chromatography-tandem mass spectrometryOsama Y Al-Dirbashi, Nathan McIntosh, Christine McRoberts, 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.Pageof 11