Submicroscopic deletions are rare in Alagille syndrome.

Samankaltaisia teoksia

• Segregation analysis of Alagille syndrome.
  Tekijä: Dhorne-Pollet, S, et al.
  Julkaistu: (1994)
• Screening of microdeletions of chromosome 20 in patients with Alagille syndrome.
  Tekijä: Desmaze, C, et al.
  Julkaistu: (1992)
• Alagille syndrome and deletion of 20p.
  Tekijä: Anad, F, et al.
  Julkaistu: (1990)
• Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.
  Tekijä: Rand, E B, et al.
  Julkaistu: (1995)
• Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions
  Tekijä: Nagai, T, et al.
  Julkaistu: (2003)