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Results: 1-24 |
Results: 24

Authors: COLEMAN MP CONFORTI L BUCKMASTER EA TARLTON A BROWN MC LYON MF PERRY VH
Citation: Mp. Coleman et al., REFINED GENETIC-MAPPING OF THE SLOW WALLERIAN DEGENERATION (WLD') CANDIDATE REGION, European journal of neuroscience, 10, 1998, pp. 7005-7005

Authors: HAYES C BROWN JM LYON MF MORRISKAY GM
Citation: C. Hayes et al., SONIC HEDGEHOG IS NOT REQUIRED FOR POLARIZING ACTIVITY IN THE DOUBLEFOOT MUTANT MOUSE LIMB BUD, Development, 125(3), 1998, pp. 351-357

Authors: YANG Y GUILLOT P BOYD Y LYON MF MCMAHON AP
Citation: Y. Yang et al., EVIDENCE THAT PREAXIAL POLYDACTYLY IN THE DOUBLEFOOT MUTANT IS DUE TOECTOPIC INDIAN HEDGEHOG SIGNALING, Development, 125(16), 1998, pp. 3123-3132

Authors: LYON MF
Citation: Mf. Lyon, X-CHROMOSOME INACTIVATION - A REPEAT HYPOTHESIS, Cytogenetics and cell genetics, 80(1-4), 1998, pp. 133-137

Authors: STEELE EC LYON MF FAVOR J GUILLOT PV BOYD Y CHURCH RL
Citation: Ec. Steele et al., A MUTATION IN THE CONNEXIN-50 (CX50) GENE IS A CANDIDATE FOR THE NO2 MOUSE CATARACT, Current eye research (Print), 17(9), 1998, pp. 883-889

Authors: COLEMAN MP CONFORTI L BUCKMASTER EA TARLTON A EWING RM BROWN MC LYON MF PERRY VH
Citation: Mp. Coleman et al., AN 85-KB TANDEM TRIPLICATION IN THE SLOW WALLERIAN DEGENERATION (WLD(S)) MOUSE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(17), 1998, pp. 9985-9990

Authors: LEHMAN AL NAKATSU Y CHING A BRONSON RT OAKEY RJ KEIPERHRYNKO N FINGER JN DURHAMPIERRE D HORTON DB NEWTON JM LYON MF BRILLIANT MH
Citation: Al. Lehman et al., A VERY LARGE PROTEIN WITH DIVERSE FUNCTIONAL MOTIFS IS DEFICIENT IN RJS (RUNTY, JERKY, STERILE) MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(16), 1998, pp. 9436-9441

Authors: HAYES C LYON MF MORRISSKAY GM
Citation: C. Hayes et al., MORPHOGENESIS OF DOUBLEFOOT (DBF), A MOUSE MUTANT WITH POLYDACTYLY AND CRANIOFACIAL DEFECTS, Journal of Anatomy, 193, 1998, pp. 81-91

Authors: BERGSTROM RA YOU Y ERWAY LC LYON MF SCHIMENTI JC
Citation: Ra. Bergstrom et al., DELETION MAPPING OF THE HEAD TILT (HET) GENE IN MICE - A VESTIBULAR MUTATION CAUSING SPECIFIC ABSENCE OF OTOLITHS, Genetics, 150(2), 1998, pp. 815-822

Authors: LYON MF
Citation: Mf. Lyon, X-CHROMOSOME INACTIVATION SPREADS ITSELF - EFFECTS IN AUTOSOMES, American journal of human genetics, 63(1), 1998, pp. 17-19

Authors: COLEMAN MP BUCKMASTER EA OGUNKOLADE BW TARLTON A LYON MF BROWN MC PERRY VH
Citation: Mp. Coleman et al., HIGH-RESOLUTION MAPPING OF THE GENES KCNB3 AND LY63 ON DISTAL MOUSE CHROMOSOME-4, Mammalian genome, 7(7), 1996, pp. 552-553

Authors: KERSCHER S GLENISTER PH FAVOR J LYON MF
Citation: S. Kerscher et al., 2 NEW CATARACT LOCI, CCW AND TO3, AND FURTHER MAPPING OF THE NPP AND OPJ CATARACTS IN THE MOUSE, Genomics, 36(1), 1996, pp. 17-21

Authors: COLEMAN MP BUCKMASTER EA OGUNKOLADE BW TARLTON A LYON MF BROWN MC PERRY VH
Citation: Mp. Coleman et al., MAPPING OF GENES ON DISTAL MOUSE CHROMOSOME-4, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 146-147

Authors: LYON MF
Citation: Mf. Lyon, X-CHROMOSOME INACTIVATION - PINPOINTING THE CENTER, Nature, 379(6561), 1996, pp. 116-117

Authors: LYON MF QUINNEY R GLENISTER PH KERSCHER S GUILLOT P BOYD Y
Citation: Mf. Lyon et al., DOUBLEFOOT - A NEW MOUSE MUTANT AFFECTING DEVELOPMENT OF LIMBS AND HEAD, Genetical Research, 68(3), 1996, pp. 221-231

Authors: LYON MF
Citation: Mf. Lyon, AN ADDITIONAL TYPE OF MALE-STERILITY AND INHERITED URINARY OBSTRUCTION IN MICE WITH THE T-HAPLOTYPE T(H7), Genetical Research, 67(3), 1996, pp. 249-256

Authors: LYON MF
Citation: Mf. Lyon, GREEN,MARGARET,C. - IN-MEMORIAM, Mammalian genome, 6(12), 1995, pp. 828-829

Authors: KERSCHER S CHURCH RL BOYD Y LYON MF
Citation: S. Kerscher et al., MAPPING OF 4 MOUSE GENES ENCODING EYE LENS-SPECIFIC STRUCTURAL, GAP JUNCTION, AND INTEGRAL MEMBRANE-PROTEINS - CRYBA1 (CRYSTALLIN-BETA-A3 A1), CRYBB2 (CRYSTALLIN-BETA-B2), GJA8 (MP70), AND LIM2 (MP19)/, Genomics, 29(2), 1995, pp. 445-450

Authors: LYON MF
Citation: Mf. Lyon, THE HISTORY OF X-CHROMOSOME INACTIVATION AND RELATION OF RECENT FINDINGS TO UNDERSTANDING OF HUMAN X-LINKED CONDITIONS, Turkish Journal of Pediatrics, 37(2), 1995, pp. 125-140

Authors: FOREJT J ARTZT K BARLOW DP HAMVAS RMJ LINDAHL KF LYON MF KLEIN J SILVER LM
Citation: J. Forejt et al., MOUSE CHROMOSOME-17, Mammalian genome, 5, 1994, pp. 238-258

Authors: LOSTER J PRETSCH W SANDULACHE R SCHMITTJOHN T LYON MF GRAW J
Citation: J. Loster et al., CLOSE LINKAGE OF THE DOMINANT CATARACT MUTATIONS (CAT-2) WITH IDH-1 AND CRYGE ON MOUSE CHROMOSOME-1, Genomics, 23(1), 1994, pp. 240-242

Authors: EVERETT CA GLENISTER PH TAYLOR DM LYON MF KRATOCHVILOVALOESTER J FAVOR J
Citation: Ca. Everett et al., MAPPING OF 6 DOMINANT CATARACT GENES IN THE MOUSE, Genomics, 20(3), 1994, pp. 429-434

Authors: REED V GEORGE AM GLENISTER PH CHELLY J MONACO AP TUMER Z HORN N CATTANACH BM LYON MF BOYD Y
Citation: V. Reed et al., ANALYSIS OF MUTATIONS AT THE MOTTLED LOCUS IN THE MOUSE, THE POSTULATED MURINE HOMOLOG OF MENKE SYNDROME, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 172-173

Authors: LYON MF OGUNKOLADE BW BROWN MC ATHERTON DJ PERRY VH
Citation: Mf. Lyon et al., A GENE AFFECTING WALLERIAN NERVE DEGENERATION MAPS DISTALLY ON MOUSE CHROMOSOME-4, Proceedings of the National Academy of Sciences of the United Statesof America, 90(20), 1993, pp. 9717-9720
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