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American Journal of Medical Genetics|August 1, 1989
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden deathV E Shih, S M Axel, J C Tewksbury, et al.
Neurology|August 28, 2002
Homocysteine, MTHFR 677C-->T polymorphism, and risk of ischemic stroke: results of a meta-analysisP J Kelly, J Rosand, J P Kistler, et al.
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.
Neurology|January 29, 2003
Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiencyP J Kelly, K L Furie, J P Kistler, et al.
American Journal of Human Genetics|February 1, 1988
The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophyV Ramesh, L A Benoit, P Crawford, et al.
Prenatal Diagnosis|May 1, 1996
Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemiaR Mandell, S Packman, R Laframboise, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophyV Ramesh, A I McClatchey, N Ramesh, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3V Ramesh, S V Cheng, C A Kozak, et al.
American Journal of Human Genetics|May 1, 1983
The prognosis of hyperlysinemia: an interim reportJ Dancis, J Hutzler, M G Ampola, et al.
American Journal of Human Genetics|November 1, 1990
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophyA I McClatchey, D L Kaufman, E L Berson, et al.
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