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Baranov, V. S (1983). Chromosomal control of early embryonic development in mice I. Experiments on embryos with autosomal monosomy. Genetica 61, 165-177.

Barton, S. C., Surani, M. A. H. and Norris, M. L (1984). Role of maternal and paternal genomes in mouse development. Nature 311, 374-376.[Medline]

Barton, S. C., Ferguson-Smith, A. C., Fundele, R. and Surani, M. A (1991). Influence of paternally imprinted genes on development. Development 113, 679-688.[Abstract]

Clouthier, D. E., Hosoda, K., Richardson, J. A., Williams, S. C., Yanagisawa, H., Kuwaki, T., Kumada, M., Hammer, R. E. and Yanagisawa, M (1998). Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. Development 125, 813-824.[Abstract]

Cockett, N. E., Jackson, S. P., Shay, T. L., Nielsen, D. M., Moore, S. S., Steele, M. R., Barendse, W., Green, R. D. and Georges, M (1994). Chromosomal localisation of the callipyge gene in sheep ( Ovis aries ) using bovine DNA markers. Proc. Natl. Acad. Sci. USA 91, 3019-3023.[Abstract/Free Full Text]

Cockett, N. E., Jackson, S. P., Shay, T. L., Farnir, F., Berghmans, S., Snowder, G. D., Nielsen, D. M. and Georges, M (1996). Polar overdominance at the ovine callipyge locus. Science 273, 236-238.[Abstract]

Cotter, P. D., Kaffe, S., McCurdy, L. D., Jhaveri, M., Willner, J. P. and Hirschhorn, K (1997). Paternal uniparental disomy for chromosome 14: a case report and review. Am. J. Med. Genet 70, 74-79.[Medline]

Dietrich, W., Katz, H., Lincoln, S. E., Shin, H-S., Friedman, J., Dracopoli, N. C. and Lander, E. S (1992). A genetic map of the mouse suitable for typing intraspecific crosses. Genetics 131, 423-447.[Abstract]

Eggenschwiler, J., Ludwig, T., Fisher, P., Leighton, P. A., Tilghman, S. M. and Efstratiadis, A (1997). Mouse mutant embryos overexpressing IGF-II exhibit features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev 11, 3128-3142.[Abstract/Free Full Text]

Efstratiadis, A (1998). Genetics of mouse growth. Int. J. Dev. Biol 42, 955-976.[Medline]

Ferguson-Smith, A. C., Sasaki, H., Cattanach, M. B. and Surani, M. A (1993). Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature 363, 751-755.

Ferguson-Smith, A. C., Cattanach, B. M., Barton, S. C., Beechey, C. M. and Surani, M. A (1991). Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature, 351, 667-670.[Medline]

Fokstuen, S., Ginsburg, C., Zachmann, M. and Schinzel, A (1999). Maternal uniparental disomy 14 as a cause of intrauterine growth retardation and early onset of puberty. J. Pediatr 134, 689-695.[Medline]

Fundele, R. H., Norris, M. L., Barton, S. C., Fehlau, M., Howlett, S. K., Mills, W. E. and Surani, M. A (1990). Temporal and spatial selection against parthenogenetic cells during development of fetal chimeras. Development 108, 203-211.[Abstract]

Fundele, R., Bober, E., Arnold, H. H., Grim, M., Bender, R., Wilting, J. and Christ, B (1994). Early skeletal muscle development proceeds normally in parthenogenetic mouse embryos. Dev. Biol 161, 30-36.[Medline]

Furst, D. O., Osborn, M. and Weber, K (1989). Myogenesis in the mouse embryo: differential onset of expression of myogenic proteins and the involvement of titin in myofibril assembly. J. Cell Biol 109, 517-527.[Abstract/Free Full Text]

Georgiades, P., Chierakul, C. and Ferguson-Smith, A. C (1998). Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting. J. Med. Genet 35, 821-824.[Abstract/Free Full Text]

Gropp, A. and Kolbus, U (1974). Exencephaly in the syndrome of trisomy no. 12 of the foetal mouse. Nature 249, 145-147.[Medline]

Gropp, A., Winking, H., Herbst, E. and Claussen, C (1983). MurineTrisomy: Developmental profiles of the embryo, and isolation of trisomic cellular systems. J. Exp. Zool 228, 253-269.[Medline]

Harris, A. J., Fitzsimons, R. B. and McEwan, J. C (1989). Neural control of the sequence of expression of myosin heavy chain isoforms in foetal mammalian muscles. Development 107, 751-769.[Abstract/Free Full Text]

Hernandez, D. and Fisher, E. M. C (1999). Mouse autosomal trisomy: two's company, three's a crowd. Trends Genet 15, 241-247.[Medline]

Lau, M. M. H., Stewart, C. E. H., Liu, Z., Bhatt, H., Rotwein, P. and Stewart, C. L (1994). Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev 8, 2953-2963.[Abstract/Free Full Text]

Ludwig, T., Eggenschwiler, J., Fisher, P., D'Ercole, A. J., Davenport, M. L. and Efstradiadis, A (1996). Mouse mutants lacking the type 2 IGF receptor (IGF2R). are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds. Dev. Biol 177, 517-535.[Medline]

Magnuson, T., Debrot, S., Dimpel, J., Zweig, A., Zamora, T. and Epstein, C. J (1985). The early lethality of autosomal monosomy in the mouse. J. Exp. Zool 263, 353-360.

Mann, J. R., Gadi, I., Harbison, M. L., Abbondanzo, S. J. and Stewart, C. L (1990). Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting. Cell 62, 251-260.[Medline]

Mann, J. R. and Stewart, C. L (1991). Development to term of mouse androgenetic aggregation chimaeras. Development 113, 1325-.[Abstract]

McGrath, J. and Solter, D (1984). Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37, 179-183.[Medline]

McLaughlin, K. J., Kochanowski, H., Solter, D., Schwarzkopf, G., Szabo,P. E. and Mann, J. R (1997). Roles of the imprinted gene Igf2 and paternal duplication of distal chromosome 7 in the perinatal abnormalities of androgenetic mouse chimeras. Development 124, 4897-4904.[Abstract]

McLeod, M. J (1980). Differential staining of cartilage and bone in whole fetuses by alcian blue and alizarin red S. Teratology 3, 299-301.

Miller, J. B (1992). Myoblast diversity in skeletal myogenesis: How much and to what end?. Cell 69, 1-3.[Medline]

Moore, T. and Haig, D (1991). Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet 7, 45-49.[Medline]

Ontell, M. and Kozeka, K (1984). The organogenesis of murine striated muscle: a cytoarchitectural study. Am. J. Anat 171, 133-148.[Medline]

Schuster-Gossler, K., Simon-Chazottes, D., Guenet, J.-L., Zachgo, J. and Gossler, A (1996). Gtl2LacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype. Mamm. Genome 7, 20-24.[Medline]

Schuster-Gossler, K., Bilinski, P., Sado, T., Ferguson-Smith, A. and Gossler, A (1998). The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA. Dev. Dynam 212, 214-228.[Medline]

Surani, M. A. H., Barton, S. C. and Norris, M. L (1984). Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308, 548-550.[Medline]

Takada, S., Tevendale, M., Baker, J., Georgiades, P., Campbell, E., Freeman, T., Johnson, M. H., Paulsen, M. and Ferguson-Smith, A. C (2000). Delta-like. and Gtl2 are reciprocally expressed, differentially methylated, linked imprinted genes on mouse chromosome 12. Curr. Biol 10, 1135-1138.[Medline]

Temple, I. K., Cockwell, A., Hassold, T., Pettay, D. and Jacobs, P (1991). Maternal uniparental disomy for chromosome 14. J. Med. Genet 28, 511-514.[Abstract/Free Full Text]

Venuti, J. M., Morris, J. H., Vivian, J. L., Olson, E. N. and Klein, W. H (1995). Myogenin is required for late but not early aspects of myogenesis during mouse development. J. Cell Biol 128, 563-576.[Abstract/Free Full Text]

Wang, J. C., Passage, M. B., Yen, P. H., Shapiro, L. J. and Mohandas, T. K (1991). Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier. Am. J. Hum. Genet 48, 1069-1074.[Medline]

Watanabe, T., Tartellin, E., Neubuser, A., Kimura, M. and Solter, D (1994). Fine genetic mapping defines the genetic order of Pax9, Tcf3a, and Acrodysplasia (Adp). Mamm. Genome 5, 768-770.[Medline]

Wigmore, P. M. and Dunglison, G. F (1998). The generation of fiber diversity during myogenesis. Int. J. Dev. Biol 42, 117-125.[Medline]

Wilson, S. J., Ross, J. J. and Harris, A. J (1988). A critical period for the formation of secondary myotubes defined by prenatal undernourishment in rats. Development 102, 815-821.[Abstract/Free Full Text]

Yan, Y., Frisen, J,. Lee, M.-H., Massague, J. and Barbacid, M (1997). Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. Genes Dev 11, 973-983.[Abstract/Free Full Text]

Zhang, M. and McLennan, I. S (1995). During secondary myotube formation primary myotubes preferentially absorb new nuclei at their ends. Dev. Dyn 204, 168-177.[Medline]

Zhang, P., Liegeois, N. J., Wong, C., Finegold, M., Hou, H., Thompson, J. C., Silverman, A., Harper, J. W., DePinho, R. A. and Elledge, S. J (1997). Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith-Wiedemann syndrome. Nature 387, 151-158.[Medline]





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