References
Apkarian, P., Spekreijse, H., VanSwaay, E., and Van Schooneveld, M.: Visual evoked potentials in Prader-Willi syndrome.Documenta Ophthalmologica 71: 355–367, 1989.
Bray, G.A., Dahms, W.T., Swerdloff, R.S., Fisher, R.H., Atkinson, R.L., and Carrel, R.E.: The Prader-Willi syndrome: A study of 40 patients and a review of the literature.Medicine 62: 59–80, 1983.
Brilliant, M.H., Gondo, Y., and Eicher, E.M.: Direct identification of the mouse pink-eyed unstable mutation by genome scanning.Science 252: 566–569, 1991.
Brilliant, M.H., Szabo, G., Katarova, Z., Kozak, C.A., Glaser, T.M., Greenspan, R.J., and Housman, D.E.: Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10.Genomics 6: 115–122, 1990.
Brumbaugh, J.A., Wilkins, L.M., and Moore, J.W.: Genetic dissection of eumelanogenesis.Pigment Cell 4: 150–158, 1979.
Butler, M.G.: Hypopigmentation: A common feature of Prader-Labbart-Willi syndrome.Am J Hum Genet 45: 140–146, 1989.
Chaillet, J.R., Knoll, J.H.M., Horsthemke, B., and Lalande, M.: The syntenic relationship of the critical deletion region for the Prader-Willi/Angelman Syndromes and proximal mouse chromosome 7.Genomics, in press, 1991.
Creel, D.J., Bendel, C.M., Wiesner, G.L., Wirtschafter, J.D., Arthur, D.C., and King, R.A.: Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.New Engl J Med 314: 1606–1609, 1986.
Donlon, T.A., Lalande, M., Wyman, A., Bruns, G., and Latt, S.A.: Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.Proc Natl Acad Sci USA 83: 4408–4412, 1989.
Fryburg, J.S., Breg, W.R., and Lindgren, V.: Diagnosis of Angelman syndrome in infants.Am J Med Genet 38: 58–64, 1991.
Heim, R.A., Dunn, D.S., Candy, S.E., Zwane, E., Kromberg, J.G.R., and Jenkins, T.: The tyrosinase-positive oculocutaneous albinism locus is not linked to the β-globin locus in man.Hum Genet 79: 89, 1988.
Hittner, H.M., King, R.A., Riccardi, V.M., Ledbetter, D.H., Borda, R.P., Ferrell, R.E., and Kretzer, F.L.: Oculocutaneous albinoidism as a manifestation of reduced neural crest derivitives in the Prader-Willi syndrome.Am J Ophthalomol 94: 328–337, 1982.
Kirkilionis, A.J., Gregory, C.A., and Hamerton, J.L.: Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).Genomics 9: 524–535, 1991.
Knoll, J.H.M., Nicholls, R.D., Magenis, R.E., Graham, J.M., Lalande, M., and Latt, S.A.: Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.Am J Med Genet 32: 285–290, 1989.
Knoll, J.H.M., Nicholls, R.D., Magenis, R.E., Glatt, K., Graham, J.M., Kaplan, L., and Lalande, M.: Angelman syndrome: Three molecular classes identified with chromosome 15q11q13-specific DNA markers.Am J Hum Genet 47: 149–155, 1990.
Laland, M., Nicholls, R.D., and Knoll, J.M.H.: A cDNA from proximal human chromosome 15q maps nearMtv-1 on mouse chromosome 7.Mouse News Lett 84: 87–88, 1989.
Magenis, R.E., Toth-Fejel, S., Allen, L.J., Black, M., Brown, M.G., Budden, S., Cohen, R., Friedman, J.M., Kalousek, D., Zonana, J., Lacy, D., LaFranchi, S., Lahr, M., Macfarlane, J., and Williams, C.P.S.: Comparison of the 15q deletions in Prader-Willi and Angelman syndrome.Am J Med Genet 35: 333–349, 1990.
Nicholls, R.D., Gottlieb, W., Avidano, K., Williams, C.A., and Driscoll, D.: Mouse chromosome mapping of clones from the PWS/AS genetic region.Mouse Genome 89: 254, 1991.
Nicholls, R.D., Knoll, J.H., Glatt, K., Hersh, J.H., Brewster, T.D., Graham, J.M., Wurster-Hill, D., Wharton, R., and Latt, S.A.: Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.Am J Med Genet 33: 66–77, 1989.
Nicholls, R.D., Knoll, J.H.M., Butler, M.G., Karam, S., and Lalande, M.: Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome.Nature 342: 281–285, 1989.
Searle, A.G., and Beechey, C.V.: Genome imprinting phenomena on mouse chromosome 7.Genet Res Camb 56: 237–244, 1991.
Silver, J. and Buckler, C.E.: Statistical considerations for linkage analysis using recombinant inbred strains and backcrosses.Proc Natl Acad Sci USA 83: 1423–1427, 1986.
Silvers, W.K.: Thep-locus (pink-eyed dilution).In The Coat Colors of Mice, pp. 90–101, Springer-Verlag, New York, 1979.
Tantravahi, U., Nicholls, R.D., Stroh, H., Ringer, S., Neve, R.L., Kaplan, L., Wharton, R., Wurster-Hill, D., Graham, Jr., J.M., Cantu, E.S., Frias, J.L., Kousseff, B.G., and Latt, S.A.: Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.Am J Med Genet 33: 78–87, 1989.
Wallis, C.E. and Beighton, P.H.: Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype.J Med Genet 26: 337–339, 1988.
Wiesner, G.L., Bendel, C.M., Olds, D.P., White, J.W., Arthur, D.C., Ball, D.W., and King, R.A.: Hypopigmentation in the Prader-Willi syndrome.Am J Hum Genet 40: 431–442, 1987.
Willems, P.J., Dijkstra, I., Brouwer, O.F., and Smit, G.P.A.: Recurrence risk in the Angelman (“happy puppet”) syndrome.Am J Med Genet 27: 773–780, 1987.
Williams, C.A., Zori, R.T., Stone, J.W., Gray, B.A., Cantu, E.S., and Ostrer, H.: Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.Am J Med Genet 35: 350–353, 1990.
Witkop, Jr., C.J., Quevedo, Jr., W.C., Fitzpatrick, T.B., and King, R.A.: Albinism.In C.R. Sciver, A. Beaudet, W.S. Sly, and D. Valle (eds.)The Metabolic Basis of Inherited Disease, pp. 2905–2947, McGraw-Hill, New York, 1990.
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Nakatsu, Y., Gondo, Y. & Brilliant, M.H. Thep locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region. Mammalian Genome 2, 69–71 (1991). https://doi.org/10.1007/BF00570442
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DOI: https://doi.org/10.1007/BF00570442