Clinical utility of chromosomal microarray and whole exome sequencing in evaluating genetic causes for pregnancy loss using products of conception specimens

Geahča maid

• Clinical utility of chromosomal microarray and whole exome sequencing in evaluating genetic causes for pregnancy loss using products of conception specimens
  Dahkki: Yadam Reddy Kanaka Durga Devi, et al.
  Almmustuhtton: (2026-03-01)
• Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios
  Dahkki: Xiaomei Shi, et al.
  Almmustuhtton: (2023-12-01)
• Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
  Dahkki: Xiaomei Shi, et al.
  Almmustuhtton: (2021-01-01)
• Molecular diagnosis of rare biallelic CDC45 gene variants causing Meier–Gorlin syndrome-7 using whole exome sequencing
  Dahkki: Jianlong Zhuang, et al.
  Almmustuhtton: (2026-01-01)
• Case Report: Prenatal diagnosis of novel compound heterozygous variants in WDR35 gene causing short-rib thoracic dysplasia 7 with or without polydactyly
  Dahkki: Jianlong Zhuang, et al.
  Almmustuhtton: (2025-01-01)