References
Dryja TP, Mukai S, Petersen R, Rappaport JM, Walton D, Yandeell DW (1989) Parental origin of mutations of the retinoblastoma gene. Nature 339:556–558
Little M, van Heyyningen V, Hastie N (1991) Dads and disomy and disease. Nature 351:609–610
Reik W, Surani MA (1989) Genomic imprinting and embryonal tumours. Nature 338:112–113
Sapienza C, Tran TH, Paquette J, McGowan R, Peterson A (1989) A methylation mouse model for mammalian genome imprinting. Prog Nucleic Acid Res Mol Biol 36:145–157
Schroeder WT, Chao LY, Dao DD, Strong LC, Pathak S, Riccardi V, Lewis HH, Saunders GF (1987) Non-random loss of maternal chromosome 11 alleles in Wilms tumours. Am J Hum Genet 40:413–120
Scott J, Cowell J, Robertson ME, Priestly LM, Wadely R, Hopkins B, Pritchard J, Bell GI, Rall LB, Graham CF, Knott TJ (1985) Insulin-like growth factor-II gene expression in Wilms tumour and embryonic tissues. Nature 317:260–262
Touchida J, Ishizaki K, Sasaki S, Nakamura Y, Ikenaga M, Kato M, Sugimot M, Kotoura Y, Yamamuro T (1989) Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma. Nature 338:156–158
Zhu X, Dunn JM, Phillips RA, Goddard AD, Paton KE, Becker A, Gallie B (1989) Preferential germline mitation of the paternal allele in retinoblastoma. Nature 340:312
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Berry, C.L. Embryonal tumours and genomic imprinting. Vichows Archiv A Pathol Anat 419, 449–450 (1991). https://doi.org/10.1007/BF01650670
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DOI: https://doi.org/10.1007/BF01650670