Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies

• Päätekijät: Min Jin Lee (Tekijä), Sang Hee Park (Tekijä), Sung Han Shim (Tekijä), Myoung-jin Moon (Tekijä), Dong Hyun Cha (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Elsevier, 2019-05-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Objective: We present prenatal diagnosis of rec(18)dup(18q)inv(18)(p11.2q21.2)pat owing to paternal pericentric inversion in a fetus. Case report: A 37-year-old woman was diagnosed with multiple anomalies on a prenatal ultrasound scan at 17 weeks and 5 days of gestation. She underwent amniocentesis...