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The Journal of Clinical Investigation|May 1, 1995
Two alpha subunit donor splice site mutations cause human trifunctional protein deficiencyJ C Brackett, H F Sims, P Rinaldo, et al.The Journal of Biological Chemistry|November 13, 1998
Decreased neonatal dietary fat absorption and T cell cytotoxicity in pancreatic lipase-related protein 2-deficient miceM E Lowe, M H Kaplan, L Jackson-Grusby, et al.Seminars in Perinatology|May 20, 1999
Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complicationsA W Strauss, M J Bennett, P Rinaldo, et al.American Journal of Obstetrics and Gynecology|December 1, 1990
Isolation and characterization of the gene from a human genome encoding 17 beta-estradiol dehydrogenase: a comparison of Jar and BeWo choriocarcinoma cell linesC A Long, G S Bauer, M E Lowe, et al.Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhoodA W Strauss, C K Powell, D E Hale, et al.Pediatric Research|September 1, 1996
Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant alleleJ D Isaacs, H F Sims, C K Powell, et al.The Journal of Clinical Investigation|October 1, 1994
A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal deathJ C Brackett, H F Sims, R D Steiner, et al.Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancyH F Sims, J C Brackett, C K Powell, et al.Pageof 6