Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis
Year: 2018
Type: article
Authors: Sarah Boissel, Catherine Fallet-Bianco, David Chitayat, Valérie Kremer, Christina Nassif, Françoise Rypens, Marie-Ange Delrue, Dorothée Dal Soglio, Luc L. Oligny, Natalie Patey, Elisabeth Flori, Mireille Cloutier, David Dyment, Philippe Campeau, Aspasia Karalis, Sonia Nizard, William D. Fraser, François Audibert, Emmanuelle Lemyre, Guy A. Rouleau, Fadi F. Hamdan, Zoha Kibar, Jacques L. Michaud
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2903679952