Screening for Microdeletions of the X-Chromosome in Non-Specific Mental Retardation [2]

Samankaltaisia teoksia

• Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
  Tekijä: Martínez, F, et al.
  Julkaistu: (2001)
• Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
  Tekijä: Martínez, F, et al.
  Julkaistu: (2004)
• A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
  Tekijä: Martínez-Garay, I, et al.
  Julkaistu: (2007)
• Screening for subtelomeric chromosome deletions in children with idiopathic mental retardation
  Tekijä: Slavotinek, A, et al.
  Julkaistu: (1997)
• Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome.
  Tekijä: Martínez-Garay, I, et al.
  Julkaistu: (2003)