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Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
The Gy mutation: another cause of X-linked hypophosphatemia in mouseM F Lyon, C R Scriver, L R Baker, et al.Genomics|September 1, 1987
Chromosome maps of man and mouse, IIIA G Searle, J Peters, M F Lyon, et al.Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal deathN Hagiwara, S E Klewer, R A Samson, et al.Development (Cambridge, England)|February 1, 1991
Isolation and characterisation of a testis-expressed developmentally regulated gene from the distal inversion of the mouse t-complexN D Mazarakis, D Nelki, M F Lyon, et al.Genomics|April 1, 1994
Mapping of six dominant cataract genes in the mouseC A Everett, P H Glenister, D M Taylor, et al.Journal of Embryology and Experimental Morphology|September 1, 1986
Lack of inactivation of a mouse X-linked gene physically separated from the inactivation centreM F Lyon, J Zenthon, E P Evans, et al.Molecular Vision|May 7, 1997
Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3E C Steele, S Kerscher, M F Lyon, et al.Cell|May 19, 1989
The t complex polypeptide 1 (TCP-1) is associated with the cytoplasmic aspect of Golgi membranesK Willison, V Lewis, K S Zuckerman, et al.Science (New York, N.Y.)|August 21, 1992
The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromesJ M Gardner, Y Nakatsu, Y Gondo, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 26, 1999
The major brain isoform of kif1b lacks the putative mitochondria-binding domainL Conforti, E A Buckmaster, A Tarlton, et al.Pageof 11