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The Journal of Pediatrics|March 1, 1978
Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studiesH L Levy, S J Sepe, D S Walton, et al.European Journal of Pediatrics|July 1, 1996
The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary reportW B Hanley, R Koch, H L Levy, et al.Journal of Inherited Metabolic Disease|December 22, 1999
Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosumE J Quackenbush, K H Kraemer, W A Gahl, et al.The Journal of Pediatrics|September 1, 1994
Maternal mild hyperphenylalaninemia: results of treated and untreated pregnancies in two sistersH L Levy, B S Goss, D K Sullivan, et al.Journal of Inherited Metabolic Disease|October 2, 2003
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnanciesS H Mudd, A Tangerman, S P Stabler, et al.Journal of Inherited Metabolic Disease|April 23, 2003
Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutationS Z Kim, E Santamaria, T E Jeong, et al.JIMD Reports|February 26, 2015
Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal CharacteristicsS E Waisbren, F Rohr, V Anastasoaie, et al.Metabolism: Clinical and Experimental|May 1, 1995
Comparison of erythrocyte uridine sugar nucleotide levels in normals, classic galactosemics, and patients with other metabolic disordersJ B Gibson, R A Reynolds, M J Palmieri, et al.American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.The Journal of Pediatrics|March 1, 1987
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomesF J Rohr, L B Doherty, S E Waisbren, et al.Pageof 14