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2. Regulation of Igf2 imprinting in development and disease. Reik W; Bowden L; Constancia M; Dean W; Feil R; Forné T; Kelsey G; Maher E; Moore T; Sun FL; Walter J Int J Dev Biol; 1996; Suppl 1():53S-54S. PubMed ID: 9087693 [No Abstract] [Full Text] [Related]
3. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. Sparago A; Cerrato F; Vernucci M; Ferrero GB; Silengo MC; Riccio A Nat Genet; 2004 Sep; 36(9):958-60. PubMed ID: 15314640 [TBL] [Abstract][Full Text] [Related]
4. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development. Weksberg R; Smith AC; Squire J; Sadowski P Hum Mol Genet; 2003 Apr; 12 Spec No 1():R61-8. PubMed ID: 12668598 [TBL] [Abstract][Full Text] [Related]
5. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Sun FL; Dean WL; Kelsey G; Allen ND; Reik W Nature; 1997 Oct; 389(6653):809-15. PubMed ID: 9349812 [TBL] [Abstract][Full Text] [Related]
6. Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. Cohen MM Am J Med Genet; 1994 Aug; 52(2):233-4. PubMed ID: 7802016 [No Abstract] [Full Text] [Related]
7. Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. Schofield PN; Joyce JA; Lam WK; Grandjean V; Ferguson-Smith A; Reik W; Maher ER Toxicol Lett; 2001 Mar; 120(1-3):151-60. PubMed ID: 11323172 [TBL] [Abstract][Full Text] [Related]
8. Wiedemann-Beckwith syndrome: genomic imprinting revisited. Weksberg R Am J Med Genet; 1994 Aug; 52(2):235-6. PubMed ID: 7802017 [No Abstract] [Full Text] [Related]
9. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes. Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200 [TBL] [Abstract][Full Text] [Related]
10. Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor. Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Lausch E; Reutzel D; Fees S; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B Nat Genet; 2005 Aug; 37(8):785-6; author reply 786-7. PubMed ID: 16049499 [No Abstract] [Full Text] [Related]
11. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355 [TBL] [Abstract][Full Text] [Related]
12. Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. Joyce JA; Lam WK; Catchpoole DJ; Jenks P; Reik W; Maher ER; Schofield PN Hum Mol Genet; 1997 Sep; 6(9):1543-8. PubMed ID: 9285792 [TBL] [Abstract][Full Text] [Related]
13. Evolution of the Beckwith-Wiedemann syndrome region in vertebrates. Paulsen M; Khare T; Burgard C; Tierling S; Walter J Genome Res; 2005 Jan; 15(1):146-53. PubMed ID: 15590939 [TBL] [Abstract][Full Text] [Related]
14. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Brown KW; Villar AJ; Bickmore W; Clayton-Smith J; Catchpoole D; Maher ER; Reik W Hum Mol Genet; 1996 Dec; 5(12):2027-32. PubMed ID: 8968759 [TBL] [Abstract][Full Text] [Related]
15. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient. Higashimoto K; Jozaki K; Kosho T; Matsubara K; Fuke T; Yamada D; Yatsuki H; Maeda T; Ohtsuka Y; Nishioka K; Joh K; Koseki H; Ogata T; Soejima H Clin Genet; 2014 Dec; 86(6):539-44. PubMed ID: 24299031 [TBL] [Abstract][Full Text] [Related]
16. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Reik W; Maher ER Trends Genet; 1997 Aug; 13(8):330-4. PubMed ID: 9260520 [TBL] [Abstract][Full Text] [Related]