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Journal of Medical Genetics|February 1, 1996
Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counsellingP Guldberg, H L Levy, K F Henriksen, et al.Clinical Genetics|May 1, 1975
Free amino acids in extracts of cultured skin fibroblasts from patients with various amino acid metabolic disordersV E Shih, R Mandell, H L Levy, et al.The Journal of Pediatrics|June 1, 1996
Maternal phenylketonuria: magnetic resonance imaging of the brain in offspringH L Levy, D Lobbregt, P D Barnes, et al.The Journal of Pediatrics|March 1, 1992
Intentional infantile ethylene glycol poisoning presenting as an inherited metabolic disorderA D Woolf, A Wynshaw-Boris, P Rinaldo, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part II: Impact; a retrospective studyA Rosenmann, C R Scriver, C L Clow, et al.American Journal of Public Health|March 1, 1991
Psychosocial factors in maternal phenylketonuria: prevention of unplanned pregnanciesS E Waisbren, S Shiloh, P St James, et al.American Journal of Medical Genetics|July 14, 2000
High cognitive outcome in an adolescent with mut- methylmalonic acidemiaL Varvogli, G M Repetto, S E Waisbren, et al.The Journal of Pediatrics|March 1, 1997
Hydroxyprolinemia: comparison of a patient and her unaffected twin sisterS Z Kim, L Varvogli, S E Waisbren, et al.Prenatal Diagnosis|July 1, 1996
Fetal ultrasonography in maternal PKUH L Levy, D Lobbregt, L D Platt, et al.Genomics|March 1, 1992
Characterization of two missense mutations in human galactose-1-phosphate uridyltransferase: different molecular mechanisms for galactosemiaJ K Reichardt, J W Belmont, H L Levy, et al.Pageof 13