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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.
The British Journal of Radiology|September 25, 2014
Impact of the introduction of weekly radiotherapy quality assurance meetings at one UK cancer centreC V Brammer, L Pettit, R Allerton, 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.
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.
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.
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