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Pediatric Research|July 17, 1998
Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A)A Fischer, K P Carmichael, J F Munnell, et al.American Journal of Diseases of Children (1960)|January 1, 1991
Intellectual development in 12-year-old children treated for phenylketonuriaC G Azen, R Koch, E G Friedman, et al.Journal of Pediatric Hematology/Oncology|April 10, 2022
Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case ReportRameshwar R Rao, Ben W Dulken, Dena R Matalon, et al.American Journal of Obstetrics and Gynecology|April 1, 1992
Maternal phenylketonuria collaborative study, obstetric aspects and outcome: the first 6 yearsL D Platt, R Koch, C Azen, et al.American Journal of Medical Genetics. Part A|January 7, 2023
Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndromeDena R Matalon, Elizabeth J Bhoj, Dong Li, et al.Molecular Genetics and Metabolism|September 26, 2000
Maternal phenylketonuria: an international studyR Koch, W Hanley, H Levy, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994R Koch, H L Levy, R Matalon, et al.European Journal of Pediatrics|July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemiaH L Levy, S E Waisbren, D Lobbregt, et al.Journal of Inherited Metabolic Disease|March 21, 1998
Neonatal neurological assessment of offspring in maternal phenylketonuriaS E Waisbren, P Chang, H L Levy, et al.American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.Pageof 12