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Pediatrics|September 1, 1983
Newborn screening for phenylketonuria: predictive validity as a function of ageE R McCabe, L McCabe, G A Mosher, et al.American Journal of Medical Genetics|July 1, 1990
Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschsprung disease)L McCabe, L D Griffin, A Kinzer, et al.Histochemistry and Cell Biology|February 7, 1998
Developmental expression of hexokinase 1 and 3 in ratsK A Coerver, S M Gray, J E Barnes, et al.American Journal of Medical Genetics|July 17, 1995
Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiencyK C Worley, E A Lindsay, W Bailey, et al.Molecular Genetics and Metabolism|March 6, 1999
Bacterial species identification after DNA amplification with a universal primer pairK M McCabe, Y H Zhang, B L Huang, et al.American Journal of Medical Genetics|November 15, 1993
Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndromeK A Ellison, E J Roth, E R McCabe, et al.Biochemical Medicine and Metabolic Biology|December 1, 1994
Hexokinase binding in ischemic and reperfused piglet brainS M Gray, V Adams, Y Yamashita, et al.Human Genetics|March 1, 1989
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningD C Jinks, M Minter, D A Tarver, et al.Genomics|December 1, 1991
Mammalian hexokinase 1: evolutionary conservation and structure to function analysisL D Griffin, B D Gelb, D A Wheeler, et al.Human Mutation|December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenitaY H Zhang, B L Huang, K Anyane-Yeboa, et al.Pageof 12