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Forensic Science International|August 21, 2003
Tunisian population data on 10 Y-chromosomal lociC Brandt-Casadevall, M Ben Dhiab, F Taroni, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|December 25, 2013
[Intra-abdominal adiposity in preterm infants: an explorative study]F Taroni, L Forzenigo, T Tondolo, et al.Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Molecular characterization of inherited carnitine palmitoyltransferase II deficiencyF Taroni, E Verderio, S Fiorucci, et al.Human Molecular Genetics|January 1, 1995
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutationsE Verderio, P Cavadini, L Montermini, et al.Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.Molecular Endocrinology (Baltimore, Md.)|February 1, 1987
Posttranscriptional regulation of albumin gene expression in Xenopus liver: evidence for an estrogen receptor-dependent mechanismA T Riegel, S C Aitken, M B Martin, et al.Scottish Medical Journal|June 4, 2013
Multiplex PCR testing requires a robust multi-disciplinary strategy to effectively manage identified cases of chlamydial conjunctivitisD Lockington, R MacDonald, S King, et al.Endocrinology|April 1, 1987
Differential induction of hepatic estrogen receptor and vitellogenin gene transcription in Xenopus laevisA T Riegel, S C Aitken, M B Martin, et al.Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Phenotype and genotype variation in primary carnitine deficiencyY Wang, S H Korman, J Ye, et al.Pageof 28