Loss of imprinting of a paternally expressed transcript, with antisense orientation to K(V)LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

Eitemau Tebyg

• A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome
  gan: Smilinich, Nancy J., et al.
  Cyhoeddwyd: (1999)
• Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome
  gan: Niemitz, Emily L., et al.
  Cyhoeddwyd: (2004)
• Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.
  gan: Viljoen, D, et al.
  Cyhoeddwyd: (1992)
• Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor
  gan: Niemitz, Emily L. , et al.
  Cyhoeddwyd: (2005)
• Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects
  gan: DeBaun, Michael R., et al.
  Cyhoeddwyd: (2002)