Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects

Míreanna comhchosúla

• Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects
  de réir: Chih-Ping Chen, et al.
  Foilsithe / Cruthaithe: (2019-09-01)
• 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound
  de réir: Chih-Ping Chen, et al.
  Foilsithe / Cruthaithe: (2016-06-01)
• Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion
  de réir: Chih-Ping Chen, et al.
  Foilsithe / Cruthaithe: (2021-01-01)
• Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects
  de réir: Chih-Ping Chen, et al.
  Foilsithe / Cruthaithe: (2020-01-01)
• Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome
  de réir: Chih-Ping Chen, et al.
  Foilsithe / Cruthaithe: (2021-07-01)