Genomic characterisation of C7orf10 in Silver-Russell syndrome patients

Benzer Materyaller

• Searching for genomic variants in the MESTIT1 transcript in Silver-Russell syndrome patients
  Yazar:: Meyer, E, ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
  Yazar:: Eggermann, T, ve diğerleri
  Baskı/Yayın Bilgisi: (2005)
• Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status
  Yazar:: MERGENTHALER, S., ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• Epigenetic mutations in 11p15 in Silver‐Russell syndrome are restricted to the telomeric imprinting domain
  Yazar:: Eggermann, T, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.
  Yazar:: Eggermann, T, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)