P596: Diagnostic challenges and phenotypic variations in chimeric genome-wide maternal and paternal uniparental disomy: A prenatal and postnatal perspective

Ítems similars

• Case report: Paternal uniparental disomy on chromosome 7 and homozygous SUGCT mutation in a fetus with overweight after birth
  per: Xiufen Bu, et al.
  Publicat: (2023-10-01)
• Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus
  per: Chih-Ping Chen, et al.
  Publicat: (2021-05-01)
• Maternal uniparental disomy for chromosome 6 in 2 prenatal cases with IUGR: case report and literature review
  per: Yan Jiang, et al.
  Publicat: (2024-01-01)
• Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome
  per: Chih-Ping Chen, et al.
  Publicat: (2022-01-01)
• Uniparental disomy: expanding the clinical and molecular phenotypes of whole chromosomes
  per: Qi Chen, et al.
  Publicat: (2023-10-01)