Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p

Ítems similars

• Tetrasomy 12p (Pallister-Killian syndrome).
  per: Schinzel, A
  Publicat: (1991)
• Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister–Killian syndrome detected by amniocentesis
  per: Chih-Ping Chen, et al.
  Publicat: (2017-12-01)
• Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature
  per: Alqahtani, Amerh Salem, et al.
  Publicat: (2019)
• Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis
  per: Francesco Libotte, et al.
  Publicat: (2016-12-01)
• Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
  per: Horn, D, et al.
  Publicat: (1995)