A rare case of partial trisomy 8q24.12-q24.3 and partial monosomy of 8q24.3: Prenatal diagnosis and clinical findings

Objective: We describe a rare case of "pure" 8q duplication diagnosed prenatally by conventional karyotyping, that was further characterized by array comparative genomic hybridization (aCGH). Case report: A 39-year-old, primigravida woman underwent amniocentesis at 23 weeks of gestation be...

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Main Authors: Simona Farcas (Author), Dragos Erdelean (Author), Flavia Anne-Elise Szekely (Author), Dan Navolan (Author), Nicoleta Andreescu (Author), Andreea Cioca (Author)
Format: Book
Published: Elsevier, 2019-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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