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Author/Creator Cloutier, Mireille

2. Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis. (July 2018)

Authors:
Boissel, Sarah; Fallet-Bianco, Catherine; Chitayat, David; Kremer, Valérie; Nassif, Christina; Rypens, Françoise; Delrue, Marie-Ange; Dal Soglio, Dorothée; Oligny, Luc; Patey, Natalie; Flori, Elisabeth; Cloutier, Mireille; Dyment, David; Campeau, Philippe; Karalis, Aspasia; Nizard, Sonia; Fraser,...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 7(2018)
Page Start:
745
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Neu–Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis. Issue 5 (5th March 2019)

Authors:
Bourque, Danielle K.; Cloutier, Mireille; Kernohan, Kristin D.; Bareke, Eric; Grynspan, David; Michaud, Jean; Boycott, Kym M.
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 5(2019)
Page Start:
813
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗