Showing results (1-10 of 27) with videos related to
Sort By:
Pageof 3
Journal of Inherited Metabolic Disease|August 1, 1998
Molecular genetic research into carbamoyl-phosphate synthase I: molecular defects and linkage markersM L SummarGenomics|March 15, 1994
Linkage mapping of the gene for type III collagen (COL3A1) to human chromosome 2q using a VNTR polymorphismG E Tiller, P A Polumbo, M L SummarGenomics|June 1, 1991
Linkage analysis of the human dopamine beta-hydroxylase geneS E Perry, M L Summar, J A Phillips, et al.Clinical Genetics|February 17, 2015
Malignancy in Noonan syndrome and related disordersP Smpokou, D J Zand, K N Rosenbaum, et al.American Journal of Human Genetics|March 16, 2007
Assessing the functional characteristics of synonymous and nonsynonymous mutation candidates by use of large DNA constructsA M Eeds, D Mortlock, R Wade-Martins, et al.Journal of Inherited Metabolic Disease|January 1, 1992
Prospective versus clinical diagnosis and therapy of acute neonatal hyperammonaemia in two sisters with carbamyl phosphate synthetase deficiencyM Tuchman, S M Mauer, R A Holzknecht, et al.American Journal of Medical Genetics|October 23, 1997
Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: additional findings or a new syndrome (ARCC-NDI)?R A Coleman, J L Van Hove, C R Morris, et al.Pediatric Research|December 13, 1997
Vascular endothelial growth factor is expressed in ovine pulmonary vascular smooth muscle cells in vitro and regulated by hypoxia and dexamethasoneJ G Klekamp, K Jarzecka, R L Hoover, et al.Human Genetics|December 1, 1996
Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfismS Raskin, J D Cogan, M L Summar, et al.Radiation Research|May 1, 1997
Alteration of transcriptional and post-transcriptional expression of gamma-glutamylcysteine synthetase by diethyl maleateK R Sekhar, M Long, J Long, et al.Pageof 3