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

Benzer Materyaller

• Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
  Yazar:: Martínez, F, ve diğerleri
  Baskı/Yayın Bilgisi: (2001)
• Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
  Yazar:: Martínez, F, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
  Yazar:: Martínez-Garay, I, ve diğerleri
  Baskı/Yayın Bilgisi: (2007)
• Screening of ′Y′ chromosome microdeletions in Iranian infertile males
  Yazar:: Ali Mohammad Malekasgar, ve diğerleri
  Baskı/Yayın Bilgisi: (2008-01-01)
• X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation
  Yazar:: Martínez F, ve diğerleri
  Baskı/Yayın Bilgisi: (2007-11-01)