Deletion of mouse t-complex distorter-1 produces an effect like that of the t-form of the distorterLYON, M. F.Genetical research. 1992, Vol 59, Num 1, pp 27-33, issn 0016-6723Article

The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genesLYON, M. F.American journal of human genetics. 1988, Vol 42, Num 1, pp 8-16, issn 0002-9297Article

Male sterility of the mouse t-complex is due to homozygosity of the distorter genesLYON, M. F.Cell (Cambridge). 1986, Vol 44, Num 2, pp 357-363, issn 0092-8674Article

Some milestones in the history of X-chromosome inactivationLYON, M. F.Annual review of genetics. 1992, Vol 26, pp 17-28, issn 0066-4197Article

Experimental work on induced mutationsLYON, M. F.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 319, Num 1194, pp 341-351, issn 0080-4622Conference Paper

Induction of congenital malformation in mice by parental irradiation: transmission to later generationsLYON, M. F; RENSHAW, R.Mutation research. 1988, Vol 198, Num 2, pp 277-283, issn 0027-5107Article

Differences in or near the responder region of complete and partial mouse t-haplotypesLYON, M. F; ZENTHON, J.Genetical research. 1987, Vol 50, Num 1, pp 29-34, issn 0016-6723Article

Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouseKERSCHER, S; GLENISTER, P. H; FAVOR, J et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 1, pp 17-21, issn 0888-7543Article

Mapping of six dominant cataract genes in the mouseEVERETT, C. A; TAYLOR, D. M; LYON, M. F et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 3, pp 429-434, issn 0888-7543Article

Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouseLYON, M. F; KING, T. R; GONDO, Y et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 15, pp 6968-6972, issn 0027-8424Article

A search for strain differences in response of mice to mutagenesis by thio-TEPALYON, M. F; GLENISTER, P. H.Mutation research. 1991, Vol 249, Num 2, pp 317-321, issn 0027-5107, 5 p.Article

The t complex polypeptide 1 (TCP-1) is associated with the cytoplasmic aspect of Golgi membranesWILLISON, K; LEWIS, V; ZUCKERMAN, K. S et al.Cell (Cambridge). 1989, Vol 57, Num 4, pp 621-632, issn 0092-8674Article

Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolutionBROCKDORFF, N; FISHER, E. M. C; ORKIN, S. H et al.Cytogenetics and cell genetics. 1988, Vol 48, Num 2, pp 124-125, issn 0301-0171Article

Age related reactivation of an X-linked geneWAREHAM, K. A; LYON, M. F; GLENISTER, P. H et al.Nature (London). 1987, Vol 327, Num 6124, pp 725-727, issn 0028-0836Article

Clonal analysis of X-chromosome inactivation and the origin of the germ line in the mouse embryoGARDNER, R. L; LYON, M. F; EVANS, E. P et al.Journal of embryology and experimental morphology. 1985, Vol 88, pp 349-363, issn 0022-0752Article

A gene affecting Wallerian nerve degeneration maps distally on mouse chromosome 4LYON, M. F; OGUNKOLADE, B. W; BROWN, M. C et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 20, pp 9717-9720, issn 0027-8424Article

The mouse pink-eyed dilution gene : association with human Prader-Willi and Angelman syndromesGARDNER, J. M; NAKATSU, Y; GONDO, Y et al.Science (Washington, D.C.). 1992, Vol 257, Num 5073, pp 1121-1124, issn 0036-8075Article

Localization of the Hprt locus by in situ hybridization and distribution of loci on the mouse X-chromosomeLYON, M. F; ZENTHON, J; BURTENSHAW, M. D et al.Cytogenetics and cell genetics. 1987, Vol 44, Num 2-3, pp 163-166, issn 0301-0171Article

Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1LYON, M. F; ZENTHON, J; EVANS, E. P et al.Immunogenetics (New York, NY). 1986, Vol 24, Num 2, pp 125-127, issn 0093-7711Article

Discrimination between the effects of X-ray irradiation of the mouse oocyte and uterus on the induction of dominant lethals and congenital anomalies. II: Localised irradiation experimentsWEST, J. D; KIRK, K. M; GOYDER, Y et al.Mutation research. 1985, Vol 149, Num 2, pp 231-238, issn 0027-5107Article

A presumed deletion covering the W and Ph loci of the mouseLYON, M. F; GLENISTER, P. H; LOUTIT, J. F et al.Genetical research. 1984, Vol 44, Num 2, pp 161-168, issn 0016-6723Article

Chromosome maps of man and mouse IIBUCKLE, V. J; EDWARDS, J. H; EVANS, E. P et al.Clinical genetics. 1984, Vol 26, Num 1, pp 1-11, issn 0009-9163Article

The prevention and avoidance of genetic disease, discussion, 29-30 April 1987EDWARDS, J. H; LYON, M. F; SOUTHERN, E. M et al.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 319, Num 1194, pp 209-367, issn 0080-4622Conference Proceedings

Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crossesBROCKDORFF, N; FISHER, E. M. C; CAVANNA, J. S et al.EMBO journal (Print). 1987, Vol 6, Num 11, pp 3291-3297, issn 0261-4189Article

The Gy mutation: another cause of X-linked hypophosphatemia in mouseLYON, M. F; SCRIVER, C. R; BAKER, L. R. I et al.Proceedings of the National Academy of Sciences of the United States of America. 1986, Vol 83, Num 13, pp 4899-4903, issn 0027-8424Article