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Cytogenetics and Cell Genetics|January 1, 1988
Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolutionN Brockdorff, E M Fisher, S H Orkin, et al.Genetical Research|December 1, 1996
Doublefoot: a new mouse mutant affecting development of limbs and headM F Lyon, R Quinney, P H Glenister, et al.Genomics|September 1, 1994
Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1J Löster, W Pretsch, R Sandulache, et al.Immunogenetics|January 1, 1988
Extent of the mouse t complex and its inversions shown by in situ hybridizationM F Lyon, J Zenthon, E P Evans, et al.The EMBO Journal|November 1, 1987
Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crossesN Brockdorff, E M Fisher, J S Cavanna, et al.Genetics|October 2, 1998
Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otolithsR A Bergstrom, Y You, L C Erway, et al.Journal of Embryology and Experimental Morphology|September 1, 1986
Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouseB L Hogan, G Horsburgh, J Cohen, et al.Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
A gene affecting Wallerian nerve degeneration maps distally on mouse chromosome 4M F Lyon, B W Ogunkolade, M C Brown, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Unusual molecular characteristics of a repeat sequence island within a Giemsa-positive band on the mouse X chromosomeJ Nasir, E M Fisher, N Brockdorff, et al.Current Eye Research|September 24, 1998
A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataractE C Steele, M F Lyon, J Favor, et al.Pageof 11