Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing

Những quyển sách tương tự

• Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
  Bằng: van der Ven, Amelie T., et al.
  Được phát hành: (2018)
• Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract
  Bằng: Westland, Rik, et al.
  Được phát hành: (2021)
• Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome
  Bằng: Qiao, Fengchang, et al.
  Được phát hành: (2021)
• Evaluation of Renal Function in Children with Congenital Scoliosis and Congenital Anomalies of the Kidney and Urinary Tract
  Bằng: Gao, Zhengchao, et al.
  Được phát hành: (2018)
• Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT)
  Bằng: Rodriguez, Maria M.
  Được phát hành: (2014)