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Clinical Dysmorphology|October 1, 1992
Autosomal dominant transmission of acrodysostosisR D Steiner, R A PagonMolecular Genetics and Metabolism|September 26, 2000
Smith-Lemli-Opitz syndrome: the first malformation syndrome associated with defective cholesterol synthesisK P Battaile, R D SteinerAmerican Journal of Ophthalmology|August 1, 1995
Corneal abnormalities in a mother and daughter with focal dermal hypoplasia (Goltz-Gorlin syndrome)G T Lueder, R D SteinerClinical Genetics|July 29, 2008
The role of evidence-based medicine and clinical trials in rare genetic disordersM C Kruer, R D SteinerMolecular and Cellular Biochemistry|February 1, 1985
Differential expression of multiple forms of arginase in cultured cellsE B Spector, R M Kern, D F Haggerty, et al.Biochemical and Biophysical Research Communications|November 26, 1986
Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genesG J Dizikes, W W Grody, R M Kern, et al.Neurology|July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaY Shapira, S D Cederbaum, P A Cancilla, et al.The Journal of Pediatrics|August 1, 1979
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuriaS D Cederbaum, K N Shaw, J Dancis, et al.The Journal of Pediatrics|January 10, 2001
Psychosocial issues and coping strategies in families affected by urea cycle disordersJ A Cederbaum, C LeMons, M Rosen, et al.Pageof 10