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

Παρόμοια τεκμήρια

• Microdeletion of LIT1 in Familial Beckwith-Wiedemann Syndrome
  ανά: Niemitz, Emily L., κ.ά.
  Έκδοση: (2004)
• Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients
  ανά: Chang, Aimee S., κ.ά.
  Έκδοση: (2005)
• Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19
  ανά: DeBaun, Michael R., κ.ά.
  Έκδοση: (2003)
• Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
  ανά: Lee, M P, κ.ά.
  Έκδοση: (1997)
• Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor
  ανά: Niemitz, Emily L. , κ.ά.
  Έκδοση: (2005)