P659: Whole-genome sequencing as a first assay has the potential to shorten diagnosis time for neurodevelopmental disorders

Lignende værker

• Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic
  af: Stephanie U. Greer, et al.
  Udgivet: (2023-06-01)
• P659: Whole-genome sequencing as a first assay has the potential to shorten diagnosis time for neurodevelopmental disorders
  af: Kate Im, et al.
  Udgivet: (2023-01-01)
• Prenatal phenotypes and pregnancy outcomes of fetuses with 17p12 microdeletions and microduplications
  af: Yuanyuan Zhang, et al.
  Udgivet: (2026-05-01)
• Application of microdeletion and microduplication screening in preimplantation genetic testing: a case report
  af: Maria Katz, et al.
  Udgivet: (2026-01-01)
• Efficiency of noninvasive prenatal testing for the detection of fetal microdeletions and microduplications in autosomal chromosomes
  af: Yuanyuan Pei, et al.
  Udgivet: (2020-08-01)