Publication: Microarrays in prenatal diagnosis
Microarrays in prenatal diagnosis
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Oneda, B., & Rauch, A. (2017). Microarrays in prenatal diagnosis. Best Practice & Research. Clinical Obstetrics & Gynaecology, 42, 53–63. https://doi.org/10.1016/j.bpobgyn.2017.01.003
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In prenatal diagnosis, chromosomal microarray (CMA) has not yet fully replaced conventional karyotyping but has rapidly become the recommended test in pregnancies with ultrasound abnormalities. In this review, we provide an overview of the published data concerning this technology and the controversies concerning its use in the prenatal setting. There is abundant evidence indicating the added detection of pathogenic abnormalities with CMA in comparison to the traditional karyotyping, especially in fetuses with multiple or isolated ult
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- Oneda, Beatrice
- Rauch, Anita
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Oneda, B., & Rauch, A. (2017). Microarrays in prenatal diagnosis. Best Practice & Research. Clinical Obstetrics & Gynaecology, 42, 53–63. https://doi.org/10.1016/j.bpobgyn.2017.01.003
