Genomic Imprinting: a New Mechanism for Disease

References

• Surani MA H. Evidences and consequences of differences between maternal and paternal genomes during embryogenesis in the mouse. Experimental Approaches to Mammalian Embryonic Development, J Rossan, R A Pederson. Cambridge University Press, Cambridge 1986; 401–35
   Google Scholar
• Solter D. Inertia of the embryonic genome in mammals. Trends Genet 1987; 3: 23–7
   Web of Science ®Google Scholar
• Solter D. Differential imprinting and expression of maternal and paternal genomes. Annu Rev Genet 1988; 22: 127–46
   PubMed Web of Science ®Google Scholar
• Kajii T, Ohama K. Androgenetic origin of hydatidiform mole. Nature 1977; 268: 633–4
   PubMed Web of Science ®Google Scholar
• Szulman A E, Philippe E, Boue J G, Boue A. Human triploidy: Association with partial hydatidiform moles and nonmolar conceptuses. Hum Pathol 1981; 12: 1016–21
   PubMed Web of Science ®Google Scholar
• Jacobs P A, Szulman A E, Funkhouser J, Matsuura J S, Wilson C C. Human triploidy: Relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole. Ann Hum Genet 1982; 46: 223–31
   PubMed Web of Science ®Google Scholar
• McFadden D E, Kalousek D K. Two different phenotypes of fetuses with chromosomal triploidy: Correlation with parental origin of the extra haploid set. Am J Med Genet 1991; 38: 535–8
   PubMed Web of Science ®Google Scholar
• McFadden D E, Kwong L C, Yam IY L, Langlois S. Parental origin of triploidy in human fetuses—evidence for genomic imprinting. Hum Genet 1993, in press.
   PubMed Web of Science ®Google Scholar
• Kaplan L C, Wharton R, Elias E, Mandell F, Donlon T, Latt S A. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance. Am J Med Genet 1987; 28: 45–53
   PubMed Web of Science ®Google Scholar
• Magenis R E, Toth-Fejel S, Allen L J, et al. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletion, parental origin, and clinical consequences. Am J Med Genet 1990; 35: 333–49
   PubMed Web of Science ®Google Scholar
• Knoll JH M, Nicholls R D, Magenis R E, Graham J M, Jr, Lalande M, Latt S A. Angelman and Prader-Willi syndromes share a common chromosome deletion but differ in parental origin of the deletion. Am J Med Genet 1989; 32: 285–90
   PubMed Web of Science ®Google Scholar
• Nicholls R D, Knoll JH M, Butler M G, Karam S, Lalande M. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature 1989; 342: 281–5
   PubMed Web of Science ®Google Scholar
• Mascari M J, Gottlieb W, Rogan P K, et al. The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. N Engl J Med 1992; 326: 1599–607
   PubMed Web of Science ®Google Scholar
• Robinson W P, Bottani A, Yagang X, et al. Molecular cytogenetic and clinical investigations of Prader-Willi syndrome patients. Am J Hum Genet 1991; 49: 1219–34
   PubMed Web of Science ®Google Scholar
• Malcolm S, Clayton-Smith J, Nichols M, et al. Uniparental paternal disomy in Angelman's syndrome. Lancet 1991; 337: 694–7
   PubMed Web of Science ®Google Scholar
• Fontaine B, Rouleau G A, Seizinger B, et al. Equal parental origin of chromosome 22 losses in human sporadic meningioma: No evidence for genomic imprinting. Am J Hum Genet 1990; 47: 823–7
   PubMed Web of Science ®Google Scholar
• Toguchida J, Ishizaki K, Sasaki M S, et al. Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma. Nature 1989; 338: 156–8
   PubMed Web of Science ®Google Scholar
• Scrable H, Cavenee W, Ghavimi F, Lovell M, Morgan K, Sapienza C. A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. Proc Natl Acad Sci USA 1989; 86: 7480–4
   PubMed Web of Science ®Google Scholar
• Pal N, Wadey R B, Buckle B, Yeomans E, Pritchard J, Cowell J K. Preferential loss of maternal alleles in sporadic Wilms' tumour. Oncogene 1990; 5: 1665–8
   PubMed Web of Science ®Google Scholar
• Feinberg A P. Genomic imprinting and gene activation in cancer. Nature Genet 1993; 4: 110–3
   PubMed Web of Science ®Google Scholar
• Rainier S, Johnson L A, Dobry C J, Ping A J, Grundy P E, Feinberg A P. Relaxation of imprinted genes in human cancer. Nature 1993; 362: 747–9
   PubMed Web of Science ®Google Scholar
• Ogawa O, Eccles M R, Szeto J, et al. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 1993; 362: 749–51
   PubMed Web of Science ®Google Scholar
• Van Der Mey AG L, Maaswinkel-Mooy P D, Cornelisse C J, Schmidt P H, Van De Kamp JJ P. Genomic imprinting in hereditary glomus tumours: Evidence for new genetic theory. Lancet 1989; 2: 1291–4
   PubMed Web of Science ®Google Scholar
• Viljoen D, Ramesar R. Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome. J Med Genet 1992; 29: 221–5
   PubMed Web of Science ®Google Scholar
• Haas O A, Argyriou-Tirita A, Lion T. Parental origin of chromosomes involved in the translocation t(9;22). Nature 1992; 359: 414–6
   PubMed Web of Science ®Google Scholar
• Searle A G, Peters J, Lyon M F, et al. Chromosome maps of man and mouse IV. Ann Hum Genet 1989; 53: 89–140
   PubMed Web of Science ®Google Scholar
• Cattanach B M, Beechey C V. Autosomal and X-chromosome imprinting. Dev Suppl 1990; 63–72
   PubMedGoogle Scholar