Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study

Objective: Prenatal diagnosis of de novo segmental amplification or deletion by microarray-based comparative genomic hybridization (array CGH) is uncommon. The study aimed to know about the incidence, abnormal ultrasound findings, and pregnancy outcomes of prenatally diagnosed de novo segmental ampl...

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Main Authors: Hsiu-Huei Peng (Author), Chien-Hong Lee (Author), Sheng-Yuan Su (Author), Kuan-Ju Chen (Author), Yen-Chang Lee (Author), Shu-Han You (Author), Wen-Fang Lee (Author), Po-Jen Cheng (Author)
Formato: Libro
Publicado: Elsevier, 2019-09-01T00:00:00Z.
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Número de Clasificación: A1234.567
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