[Does the prevalence of recurrent pathogenic microdeletions and microdoublements in prenatal diagnosis lead to a reassessment of the evolution of non-invasive screening techniques? The example of region 22q11.2]

Gynecol Obstet Fertil Senol. 2017 Jan;45(1):45-49. doi: 10.1016/j.gofs.2016.12.014. Epub 2017 Jan 18.
[Article in French]
No abstract available

Publication types

  • Comment

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome
  • Female
  • Gene Deletion
  • Heart Defects, Congenital
  • Humans
  • In Situ Hybridization, Fluorescence
  • Phenotype
  • Pregnancy
  • Prenatal Diagnosis*
  • Prevalence