Showing results (71-80 of 494) with videos related to
Sort By:
Pageof 50
European Journal of Pediatrics|December 1, 1978
Delayed cutaneous hypersensitivity in children with severe multiple handicaps treated with phenytoinA Higashi, I Matsuda, S Sinosuka, et al.American Journal of Medical Genetics|March 17, 1997
Familial lethal inheritance of a mutated paternal gene in females causing X-linked ornithine transcarbamylase (OTC) deficiencyS Komaki, T Matsuura, K Oyanagi, et al.Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica|October 14, 2000
[High-throughput techniques for analyzing SNPs and application of SNPs to pharmacogenomics]A TanoueHuman Gene Therapy|May 1, 1996
Correction of ornithine transcarbamylase deficiency in adult spf(ash) mice and in OTC-deficient human hepatocytes with recombinant adenoviruses bearing the CAG promoterK Kiwaki, Y Kanegae, I Saito, et al.Kidney International|November 1, 1994
Mutations in the COL4A5 gene in Alport syndrome: a possible mutation in primordial germ cellsH Nakazato, S Hattori, T Ushijima, et al.Clinical Genetics|November 27, 1998
X-inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiencyT Yorifuji, J Muroi, A Uematsu, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 12, 1982
Skin histidase activity and urine formiminoglutamic acid (FIGLU) in patients with histidinemia found by screening newborn infantsI Matsuda, K Matsuo, F Endo, et al.Kidney International|November 5, 1997
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuriaH Nakazato, S Hattori, A Furuse, et al.Genomics|December 1, 1996
Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2)R Hoshide, Y Ikeda, S Karashima, et al.Clinical Genetics|August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B diseaseN Ishii, T Oohira, A Oshima, et al.Pageof 50