X-chromosome inactivation and human genetic disease von Lyon, MF

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LINE-1 Elements and X Chromosome Inactivation: A Function for "Junk" DNA? von Lyon, Mary F.

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X-Chromosome inactivation: a repeat hypothesis von Lyon, M.F.

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TRANSMISSION RATIO DISTORTION IN MICE von Lyon, Mary F

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A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding von Lyon, Mary F., Jamieson, Robyn V., Perveen, Rahat, Glenister, Peter H., Griffiths, Robert, Boyd, Yvonne, Glimcher, Laurie H., Favor, Jack, Munier, Francis L., Black, Graeme C. M.

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The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes von LYON, M. F

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The Lyon and the LINE hypothesis von Lyon, Mary F

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The Scurfy Mouse Mutant has Previously Unrecognized Hematological Abnormalities and Resembles Wiskott-Aldrich Syndrome von Lyon, M. F., Peters, J., Glenister, P. H., Ball, S., Wright, E.

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Some Milestones in the History of X-Chromosome Inactivation von Lyon, Mary F

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X-chromosome inactivation von Lyon, Mary F

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X-Chromosome Inactivation Spreads Itself: Effects in Autosomes von Lyon, Mary F.

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Genetic and Molecular Analysis of Recessive Alleles at the Pink-Eyed Dilution (p) Locus of the Mouse von Lyon, Mary F., King, Thomas R., Gondo, Yoichi, Gardner, John M., Nakatsu, Yoshimichi, Eicher, Eva M., Brilliant, Murray H.

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Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse von HOGAN, B. L. M, HORSBURGH, G, COHEN, J, HETHERINGTON, C. M, FISHER, G, LYON, M. F

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Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouse von KERSCHER, S, GLENISTER, P. H, FAVOR, J, LYON, M. F

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An 85-kb Tandem Triplication in the Slow Wallerian Degeneration (Wlds) Mouse von Coleman, Michael P., Conforti, Laura, Buckmaster, E. Anne, Tarlton, Andrea, Ewing, Robert M., Brown, Michael C., Lyon, Mary F., Perry, V. Hugh

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Male sterility of the mouse t-complex is due to homozygosity of the distorter genes von Lyon, Mary F.

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Age related reactivation of an X-linked gene von Wareham, Kathryn A, Lyon, Mary F, Glenister, P. H, Williams, E. D

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The Gy Mutation: Another Cause of X-Linked Hypophosphatemia in Mouse von Lyon, M. F., Scriver, C. R., Baker, L. R. I., Tenenhouse, H. S., Kronick, J., Mandla, S.

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