Noninvasive prenatal testing aids identification of tetrasomy 18p: A case report

• Asıl Yazarlar: Yuko Tamaki (Yazar), Yukiko Katagiri (Yazar), Nahomi Umemura (Yazar), Naoki Takeshita (Yazar), Mineto Morita (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Elsevier, 2020-07-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Tetrasomy 18p syndrome (Online Mendelian Inheritance in Man 614290) is a rare chromosomal disorder that is seen in approximately 1 in every 180,000 live births. It is caused by the presence of isochromosome 18p, which is a supernumerary marker composed of two copies of the short arms of chromosome 1...