Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype

Lignende værker

• Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies
  af: Iourov, Ivan Y, et al.
  Udgivet: (2012)
• Array-CGH testing in spontaneous abortions with normal karyotypes
  af: Cleide L. Borovik, et al.
  Udgivet: (2008-01-01)
• A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
  af: Yin, Aihua, et al.
  Udgivet: (2014)
• Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
  af: Shaw-Smith, C, et al.
  Udgivet: (2004)
• Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies
  af: Uwineza, Annette, et al.
  Udgivet: (2014)