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Nursing Economic$|May 1, 1993
Discovering work excitement among navy nursesS Savage, L M Simms, R A Williams, et al.The Journal of Pediatrics|March 1, 1992
Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyA Davidson-Mundt, A S Luder, C L GreeneAmerican Journal of Medical Genetics|November 15, 1993
Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: implications for evaluation of new therapiesG A McDowell, T M Cowan, M G Blitzer, et al.The Journal of Pediatrics|October 1, 1993
Molybdenum cofactor deficiencyG L Arnold, C L Greene, J P Stout, et al.Journal of the National Cancer Institute|December 1, 1982
Probable clonal origin of neurofibrosarcoma in a patient with hereditary neurofibromatosisJ M Friedman, P J Fialkow, C L Greene, et al.American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|December 1, 1996
Radiocephalometric evaluation of a family with mandibulofacial dysostosisS Bhatia, M S Block, D R Hoffman, et al.Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2000
GABA receptor antagonists modulate postmitotic cell migration in slice cultures of embryonic rat cortexT N Behar, A E Schaffner, C A Scott, et al.American Journal of Human Genetics|September 1, 1993
Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolismB A Citron, S Kaufman, S Milstien, et al.Journal of Inherited Metabolic Disease|January 24, 2004
Markedly elevated serum biotinidase activity may indicate glycogen storage disease type IaB Wolf, C L Freehauf, J A Thomas, et al.Journal of Neurogenetics|April 1, 1984
3-Hydroxy-3-methylglutaric aciduriaC L Greene, H M Cann, B H Robinson, et al.Pageof 4