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Molecular Genetics and Metabolism|May 15, 2001
Functional analysis of novel mutations in a congenital disorder of glycosylation Ia patient with mixed Asian ancestryV Westphal, G M Enns, M F McCracken, et al.Clinical Neuropathology|April 10, 2009
A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathyB C Mobley, G M Enns, L-J Wong, et al.Journal of Inherited Metabolic Disease|May 20, 2005
Management of methylmalonic acidaemia by combined liver-kidney transplantationS Nagarajan, G M Enns, M T Millan, et al.Molecular Genetics and Metabolism|August 4, 2010
Suboptimal outcomes in patients with PKU treated early with diet alone: revisiting the evidenceG M Enns, R Koch, V Brumm, et al.American Journal of Medical Genetics|December 18, 1998
Severe congenital anomalies requiring transplantation in children with Kabuki syndromeA Ewart-Toland, G M Enns, V A Cox, et al.Molecular Genetics and Metabolism|July 12, 2003
Congenital disorder of glycosylation Ic in patients of Indian originJ W Newell, N-S Seo, G M Enns, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|January 30, 2009
Successful pregnancy and cesarean delivery via noninvasive ventilation in mitochondrial myopathyN Yuan, Y Y El-Sayed, S J Ruoss, et al.American Journal of Medical Genetics|October 27, 1998
Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature reviewG M Enns, V A Cox, R B Goldstein, et al.American Journal of Medical Genetics|September 14, 1999
Apparent cyclophosphamide (cytoxan) embryopathy: a distinct phenotype?G M Enns, E Roeder, R T Chan, et al.Journal of Inherited Metabolic Disease|July 10, 1999
Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalaminG M Enns, A J Barkovich, D S Rosenblatt, et al.Pageof 2