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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.Gene|January 1, 1986
Functional analysis of the human tissue-type plasminogen activator protein: the light chainM E MacDonald, A J van Zonneveld, H PannekoekBlood|September 1, 1980
Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiationJ F Gusella, S C Weil, A S Tsiftsoglou, et al.Nature Genetics|January 1, 1993
Neurofibromatosis type 1 gene mutations in neuroblastomaI The, A E Murthy, G E Hannigan, et al.American Journal of Medical Genetics|February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosisJ L Haines, W L Yan, R M Boustany, et al.Community Dentistry and Oral Epidemiology|July 18, 2023
Oral health-related stigma: Describing and defining a ubiquitous phenomenonJ Doughty, M E Macdonald, V Muirhead, et al.Cancer Research|December 16, 1998
A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter creates an Ets binding site and augments transcriptionJ L Rutter, T I Mitchell, G Butticè, 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.Genomics|September 1, 1990
A genetic linkage map of chromosome 17J L Haines, L J Ozelius, H McFarlane, 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.Pageof 29