Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation

Ítems similars

• Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions
  per: Nagai, T, et al.
  Publicat: (2003)
• Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation
  per: Rio, M, et al.
  Publicat: (2002)
• Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome
  per: Miyake, Noriko, et al.
  Publicat: (2003)
• Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.
  per: Wilkie, A O
  Publicat: (1993)
• Absence of subtelomeric rearrangements in selected patients with mental retardation as assessed by multiprobe T FISH
  per: dos Santos, Suely Rodrigues, et al.
  Publicat: (2012)