Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP (2002) Am J Hum Genet 70: 604-11 Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor. Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR (2005) Am J Hum Genet 77: 887-91 Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome. Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP (1997) Am J Hum Genet 61: 304-9 Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. DeBaun MR, Niemitz EL, Feinberg AP (2003) Am J Hum Genet 72: 156-60 Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP (2004) Am J Hum Genet 75: 844-9 Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP (1999) Proc Natl Acad Sci U S A 96: 5203-8 Reduced expression of the cyclin-dependent kinase inhibitor gene p57KIP2 in Wilms' tumor. Thompson JS, Reese KJ, DeBaun MR, Perlman EJ, Feinberg AP (1996) Cancer Res 56: 5723-7 Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. Chang AS, Moley KH, Wangler M, Feinberg AP, Debaun MR (2005) Fertil Steril 83: 349-54 Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia. Clericuzio CL, Chen E, McNeil DE, O'Connor T, Zackai EH, Medne L, Tomlinson G, DeBaun M (2003) J Pediatr 143: 270-2 Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome. DeBaun MR, Siegel MJ, Choyke PL (1998) J Pediatr 132: 401-4 Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry. DeBaun MR, Tucker MA (1998) J Pediatr 132: 398-400 Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. Lennerz JK, Timmerman RJ, Grange DK, DeBaun MR, Feinberg AP, Zehnbauer BA (2010) J Mol Diagn 12: 576-88 Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome. Choyke PL, Siegel MJ, Oz O, Sotelo-Avila C, DeBaun MR (1998) AJR Am J Roentgenol 171: 733-7 Hypoglycemia in Beckwith-Wiedemann syndrome. DeBaun MR, King AA, White N (2000) Semin Perinatol 24: 164-71 Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registry. Wangler MF, Chang AS, Moley KH, Feinberg AP, Debaun MR (2005) Am J Med Genet A 134A: 187-91 LIT1 and H19 methylation defects in isolated hemihyperplasia. Martin RA, Grange DK, Zehnbauer B, Debaun MR (2005) Am J Med Genet A 134A: 129-31 Inheritance pattern of Beckwith-Wiedemann syndrome is heterogeneous in 291 families with an affected proband. Wangler MF, An P, Feinberg AP, Province M, Debaun MR (2005) Am J Med Genet A 137: 16-21 Joint laxity, scoliosis, and thoracic cage abnormalities in children with Beckwith-Wiedemann syndrome. Gerber LH, Chaudhry U, DeBaun M (2001) Eur J Pediatr 160: 143-4 Feasibility of partial nephrectomy for Wilms' tumor in children with Beckwith-Wiedemann syndrome who have been screened with abdominal ultrasonography. McNeil DE, Langer JC, Choyke P, DeBaun MR (2002) J Pediatr Surg 37: 57-60
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