| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8925354 | Journal of Gynecology Obstetrics and Human Reproduction | 2017 | 9 Pages |
Abstract
Transferring aCGH to a prenatal diagnosis at the Lyon university-hospital has increased the detection rate of chromosomal abnormalities by 4.2% compared to the single karyotype.
Keywords
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Authors
L. Pons, M. Till, E. Alix, C. Abel, D. Boggio, A. Bordes, J. Caloone, F.C. Raskin, N. Chatron, M.-P. Cordier, A. Fichez, A. Labalme, C. Lajeunesse, Ã. Liaras, M. Massoud, J. Miribel, E. Ollagnon, C. Schluth-Bolard, D. Sanlaville,