Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status

Παρόμοια τεκμήρια

• Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.
  ανά: Eggermann, T, κ.ά.
  Έκδοση: (1998)
• Epigenetic mutations in 11p15 in Silver‐Russell syndrome are restricted to the telomeric imprinting domain
  ανά: Eggermann, T, κ.ά.
  Έκδοση: (2006)
• Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
  ανά: Eggermann, T, κ.ά.
  Έκδοση: (2005)
• Genomic characterisation of C7orf10 in Silver-Russell syndrome patients
  ανά: Meyer, E, κ.ά.
  Έκδοση: (2003)
• The centromeric 11p15 imprinting centre is also involved in Silver–Russell syndrome
  ανά: Schönherr, Nadine, κ.ά.
  Έκδοση: (2007)