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Results:
1-9
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Results: 9
Authors:
Lyon, MF
Bogani, D
Boyd, Y
Guillot, P
Favor, J
Citation: Mf. Lyon et al., Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop), MOL VIS, 6(25), 2000, pp. 199-203
Authors:
Lyon, MF
Citation: Mf. Lyon, An answer to a complex problem: cloning the mouse t-complex responder, MAMM GENOME, 11(10), 2000, pp. 817-819
Authors:
Willison, KR
Lyon, MF
Citation: Kr. Willison et Mf. Lyon, A UK-centric history of studies on the mouse t-complex, INT J DEV B, 44(1), 2000, pp. 57-63
Authors:
Hagiwara, N
Klewer, SE
Samson, RA
Erickson, DT
Lyon, MF
Brilliant, MH
Citation: N. Hagiwara et al., Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death, P NAS US, 97(8), 2000, pp. 4180-4185
Authors:
Lyon, MF
Citation: Mf. Lyon, LINE-1 elements and X chromosome inactivation: A function for "junk" DNA?, P NAS US, 97(12), 2000, pp. 6248-6249
Authors:
Lyon, MF
Schimenti, JC
Evans, EP
Citation: Mf. Lyon et al., Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions, GENETICS, 155(2), 2000, pp. 793-801
Authors:
Lyon, MF
Citation: Mf. Lyon, X-chromosome inactivation, CURR BIOL, 9(7), 1999, pp. R235-R237
Authors:
Conforti, L
Buckmaster, EA
Tarlton, A
Brown, MC
Lyon, MF
Perry, VH
Coleman, MP
Citation: L. Conforti et al., The major brain isoform of Kif1b lacks the putative mitochondria-binding domain, MAMM GENOME, 10(6), 1999, pp. 617-622
Authors:
Boyd, Y
Evans, EP
Lyon, MF
Peters, J
Citation: Y. Boyd et al., Bruce Cattanach: Mutagenesis and where it can lead you, GENET RES, 72(3), 1998, pp. 175-176
Risultati:
1-9
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