Tetrasomy 12p (Pallister-Killian syndrome).

Samankaltaisia teoksia

• Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister–Killian syndrome detected by amniocentesis
  Tekijä: Chih-Ping Chen, et al.
  Julkaistu: (2017-12-01)
• Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p
  Tekijä: Davidsson, Josef, et al.
  Julkaistu: (2016)
• Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature
  Tekijä: Alqahtani, Amerh Salem, et al.
  Julkaistu: (2019)
• Pallister-Killian syndrome
  Tekijä: Srinivasan, Aarthi, et al.
  Julkaistu: (2014)
• Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis
  Tekijä: Francesco Libotte, et al.
  Julkaistu: (2016-12-01)