Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome

Similar Items

• 45,X/46,XX at the first amniocentesis, and 45,X/47,XXX/46,XX at the repeat amniocentesis and at birth in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the 45,X cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
  by: Chih-Ping Chen, et al.
  Published: (2023-11-01)
• High-level mosaicism for 45,X in 45,X/46,X,+mar at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for Turner syndrome, normal male external genitalia and positive SRY in the fetus, a favorable fetal outcome, postnatal decrease of the 45,X cell line and cytogenetic discrepancy in various tissues
  by: Chih-Ping Chen, et al.
  Published: (2023-09-01)
• A Rare Karyotype of Turner Syndrome: 45.X/47.XXX
  by: Ayça Altıncık, et al.
  Published: (2014-04-01)
• Phenotypic variability and management of patients with mosaic monosomy X and Y chromosome material: a case series
  by: Myriam Ben Fredj, et al.
  Published: (2024-05-01)
• Implicação reprodutiva do mosaicismo 59,X0/60,XX/61,XXX em bovinos
  by: Rita Maria Ladeira Pires, et al.
  Published: (2013-12-01)