NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome

Similar Items

• Cornelia de Lange Syndrome with NIPBL Gene Mutation: A Case Report
  od: Park, Kyung-Hee, i dr.
  Izdano: (2010)
• Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome
  od: Kuzniacka, Alina, i dr.
  Izdano: (2012)
• De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
  od: Thanh, Duong Chi, i dr.
  Izdano: (2020)
• Cornelia de Lange Syndrome: A Newborn with Imperforate Anus and a NIPBL Mutation
  od: Mende, Rose H., i dr.
  Izdano: (2012)
• Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
  od: Krantz, Ian D, i dr.
  Izdano: (2004)