Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2813428 | Diagnóstico Prenatal | 2012 | 15 Pages |
Abstract
The combination of the increased capacity of microarrays in screening of the human genome to detect changes in copy numbers variations, within a single experimental assay, as well as their greater technical resolution in cases of high-risk pregnancies, could lead to array-CGH to be a very interesting diagnostic approach in the next decade to replace the karyotype as a gold standard in such prenatal studies.
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Authors
MarÃa de los Ángeles Mori, Elena Mansilla, Fe GarcÃa-Santiago, Elena VallespÃn, MarÃa Palomares, Rubén MartÃn, Roberto RodrÃguez, Cristina MartÃnez-Payo, Belén Gil-Fournier, Soraya Ramiro, Pablo Lapunzina, Julián Nevado,