Inheritance Pattern of Beckwith–Wiedemann Syndrome Is Heterogeneous in 291 Families with an Affected Proband

Podobné jednotky

• Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome
  Autor: Niemitz, Emily L., a další
  Vydáno: (2004)
• Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients
  Autor: Chang, Aimee S., a další
  Vydáno: (2005)
• Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19
  Autor: DeBaun, Michael R., a další
  Vydáno: (2002)
• Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
  Autor: Lee, M P, a další
  Vydáno: (1997)
• Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor
  Autor: Niemitz, Emily L. , a další
  Vydáno: (2005)