Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO

Genomics

Volumn 34, Issue 3, 1996, Pages 299-303

  Griffith, Andrew J ^a,b   Burgess, Daniel L ^a   Kohrman, David C ^a   Yu, Jennifer ^a   Blaschak, Jillian ^b   Blanton, Susan H ^c   Boehnke, Michael ^b   Hecht, Jacqueline T ^d   Overhauser, Joan ^e   Meisler, Miriam H ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^e THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 18Q; CLEFT LIP PALATE; CLEFT PALATE; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; FEMALE; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYBRID CELL; INNER EAR MALFORMATION; MALE; MOUSE; NONHUMAN; PEDIGREE ANALYSIS; PRIORITY JOURNAL; TRANSGENE;

ANIMALIA; ATAXIA;

EID: 0030585758     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0290     Document Type: Article

References (23)

1. Burgess, D. L. (1996). "Transgenic Insertional Mutants of the Mouse Genes twirler (Tw) and Motor Endplate Disease (med)," Ph.D. Thesis, University of Michigan.
2. Green, P. (1990). Documentation for CRI-MAP, Version 2.4, unpublished computer documentation.
3. Griffith, A. J., Radice, G. L., Burgess, D. L., Kohrman, D. C., Hansen, G. M., Justice, M., Johnson, K. R. , Davisson, M., and Meisler, M. H. (1996). Location of the 9257 and ataxia mutations on mouse Chromosome 18. Mamm. Genome 7, in press.
4. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-1994 Généthon human genetic linkage map. Nature Genet. 7: 246-339.
5. Hecht, J. T., Wang, Y. P., Blanton, S. H., Michels, V. V., and Daiger, S. P. (1991a). Cleft lip and palate: No evidence of linkage to transforming growth factor alpha. Am. J. Hum. Genet. 49: 682-686.
6. Hecht, J. T., Wang, Y., Connor, B., Blanton, S. H., and Daiger, S. P. (1993). Nonsyndromic cleft lip and palate: No evidence of linkage to HLA or factor 13A. Am. J. Hum. Genet. 52: 1230-1233.
7. Hecht, J. T., Yang, P., Michels, V. V., and Buetow, K. H. (1991b). Complex segregation analysis of nonsyndromic cleft lip and palate. Am. J. Hum. Genet. 49: 674-681.
8. Johnson, K. R., and Davisson, M. T. (1996). Mouse chromosome 18. Mamm. Genome 6:Suppl.
9. Kline, A. D., Rojas, K., Mewar, R., Moshinsky, D., and Overhauser, J. (1992). Somatic cell hybrid deletion map of human chromosome 18. Genomics 13: 1-6.
10. Lander, E. S., and Green, P. (1987). Construction of multi-locus linkage maps in humans. Proc. Natl. Acad. Sci. USA 84: 2263-2267.
11. Lyon, M. F. (1955). Ataxia - A new recessive mutant of the house mouse. J. Hered. 46: 77-80.
12. Lyon, M. F. (1958). Twirler: A mutant affecting the inner ear of the house mouse. J. Embryol. Exp. Morphol. 6: 105-116.
13. Lyon, M. F. (1975). Recombination between Tw and ax. Mouse News Lett. 52: 36.
14. Murray, J. C., Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Manion, F., Quillen, J., Sheffield, V. C., Sunden, S., Duyk, G. M., Weissenbach, J., Gyapay, G., Dib, C., Morrissette, J., Lathrop, G. M., Vignal, A., White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S., Ward, D., Dausset, J., Cohen, D., and Cann, H. (1994). A comprehensive human linkage map with centimorgan density. Science 265: 2049-2054.
15. Ott, J. (1991). "Analysis of Human Genetic Linkage," Johns Hopkins Univ. Press, Baltimore, MD.
16. Overhauser, J., Mewar, R., Rojas, K., Lia, K., Kline, A. D., and Silverman, G. A. (1993). STS map of genes and anonymous DNA fragments on human chromosome 18 using a panel of somatic cell hybrids. Genomics 15: 387-391.
17. Overhauser, J., Silverman, G. A., and Geurts van Kessel, A. (1995). Third international workshop on human chromosome 18 mapping 1995. Cytogenet. Cell Genet. 71: 105-119.
18. Pierce, J. C., Sauer, B., and Sternberg, N. (1992). A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: Improved cloning efficiency. Proc. Natl. Acad. Sci. USA 89: 2056-2060.
19. Rojas, K., Silverman, G. A., Hudson, J. R., Jr., and Overhauser, J. (1995). Integration of the 1993-94 Généthon genetic linkage map for chromosome 18 with a physical map using a somatic cell hybrid mapping panel. Genomics 25: 329-330.
20. Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989). "Molecular Cloning: A Laboratory Manual," 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
21. Ting, C.-N., Burgess, D. L., Chamberlain, J. S., Keith, T. P., Falls, K., and Meisler, M. H. (1993). Phosphoenolpyruvate carboxykinase (GTP): Characterization of the human PCK1 gene and localization distal to MODY on chromosome 20. Genomics 16: 698-706.
22. Ting, C.-N., Kohrman, D., Burgess, D. L., Boyle, A., Altschuler, R. A., Gholizadeh, G., Samuelson, L. C., Jang, W., and Meisler, M. H. (1994). Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities. Genetics 136: 247-254.
23. Wallace, M. R., Andersen, L. B., Saulino, A. M., Gregory, P. E., Glover, T. W., and Collins, F. S. (1991). A de novo Alu insertion results in neurofibromatosis type 1. Nature 353: 864-866.