The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization

Genomics

Volumn 37, Issue 2, 1996, Pages 238-241

  Uwechue, Ifeanyi C ^a   Cooper, Benjamin F ^b   Goble, Corintha ^c   Hacker, T ^a   Blair, Helen J ^a   Burke, David T ^c   Herman, Gail ^b   Boyd, Yvonne ^a  

^a MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DYSKERATOSIS; FEMALE; GENE MUTATION; GENETIC RECOMBINATION; HISTOLOGY; MALE; MOUSE; MUTANT; NEWBORN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME;

ANIMALIA;

EID: 0030588153     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0549     Document Type: Article

References (10)

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2. 2. Cattanach, B. M. (1982). Research News: A new X-linked mutation. Mouse News Lett. 66: 61-62.
3. 3. Cattanach, B. M. (1982). Research News: Location of tattered (Td). Mouse News Lett. 67: 19.
4. 4. Derry, J. M. J., Ochs, J. D., and Francke, U. (1994). Isolation of a novel gene mutated in the Wiskott-Aldrich syndrome. Cell 78: 635-644.
5. 5. Dietrich, W. F., Miller, J., Steen, R., Merchant, M. A., Damron-Boles, D., Husain, Z., Dredge, R., Daly, M. J., Ingalls, K. A., O'Connor, T. J., Evans, C. A., De Angelis, M. M., Levinson, N. A., Krugylak, L., Goodman, N., Copeland, N. G., Jenkins, N. A., Hawkins, T. L., Stein, L., Page, D. C., and Lander, E. S. (1996). A comprehensive genetic map of the mouse genome. Nature 380: 149-152.
6. 6. Geraghty, M. T., Brody, L. C., Martin, L. S., Marble, M., Kearns, W., Pearson, P., Monaco, A. P., Lehrach, H., and Valle, D. (1993). The isolation of cDNAs from OATL1 at Xp11.2 using a 480-kb YAC. Genomics 16: 440-446.
7. 7. Gorski, J. L., Burright, E. N., Harnden, C. E., Stein, C. K., Glover, T. W., and Reyner, E. L. (1991). Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X chromosomal translocation breakpoints. Am. J. Hum. Genet. 48: 53-64.
8. 8. Hatchwell, E. (1994). D. Phil thesis, University of Oxford.
9. 9. Merrell, K., Gonzales, J. C., Wells, S., Calamel, K., and Herman, G. E. (1995). Genetic analysis of tattered, an X-linked dominant, developmental mouse mutation. Mamm. Genome 6: 291-294.
10. 10. Nelson, D., Ballabio, A., Cremers, F., Monaco, A. P., and Schlessinger, D. (1995). Report of the sixth international workshop on X chromosome mapping 1995. Cytogenet. Cell Genet. 71: 308-342.