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Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.American Journal of Public Health|December 1, 1982
Prevention of mental retardation in offspring of hyperphenylalaninemic mothersL Cartier, C L Clow, A Lippman-Hand, et al.Journal of Inherited Metabolic Disease|January 1, 1992
Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetusD Chitayat, A Balbul, V Hani, et al.American Journal of Medical Genetics|May 1, 1990
Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicineB R Akerman, T M Fujiwara, G A Lancaster, et al.The Journal of Pediatrics|November 1, 1987
Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.Annals of Clinical Biochemistry|November 1, 1992
Measurement of sialic acid in serum and urine: clinical applications and limitationsP J Waters, E Lewry, C A PennockAmerican Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"C R Scriver, D E Cole, S A Houghton, et al.Bone|January 31, 2004
Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp miceZ Q Qiu, R Travers, F Rauch, et al.Pageof 19