Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities

Lignende værker

• Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
  af: Cai, Meiying, et al.
  Udgivet: (2020)
• Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome
  af: Cai, Meiying, et al.
  Udgivet: (2018)
• SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis
  af: Huang, Hailong, et al.
  Udgivet: (2021)
• Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes
  af: Cai, Meiying, et al.
  Udgivet: (2021)
• Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease
  af: Xue, Huili, et al.
  Udgivet: (2021)