Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies
Objective: The objective of this study was to characterize the genetic abnormalities in two fetuses with congenital anomalies in prenatal screening. Materials and methods: The mother of Fetus 1 was 26 years old and had a second trimester serum screening that indicated the fetus was at low risk. The...
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Asıl Yazarlar: | , , , , |
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Materyal Türü: | Kitap |
Baskı/Yayın Bilgisi: |
Elsevier,
2014-12-01T00:00:00Z.
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Internet
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Yer Numarası: |
A1234.567 |
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Kopya Bilgisi 1 | Kütüphanede |