Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

Lignende værker

• Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
  af: Shaffer, Lisa G, et al.
  Udgivet: (2012)
• Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH
  af: Neill, Nicholas J., et al.
  Udgivet: (2011)
• Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report
  af: Traylor, Ryan N, et al.
  Udgivet: (2009)
• Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications
  af: Rosenfeld, Jill A., et al.
  Udgivet: (2009)
• The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
  af: Callaway, Jonathan L A, et al.
  Udgivet: (2013)