Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

समान संसाधन

• Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature
  द्वारा: Evangelidou, Paola, और अन्य
  प्रकाशित: (2013)
• Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
  द्वारा: Sismani, Carolina, और अन्य
  प्रकाशित: (2008)
• Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test
  द्वारा: Kypri, Elena, और अन्य
  प्रकाशित: (2019)
• Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.
  द्वारा: Maria C Neofytou, और अन्य
  प्रकाशित: (2017-01-01)
• Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications
  द्वारा: Neofytou, Maria C., और अन्य
  प्रकाशित: (2017)