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Author/Creator Merner, Nancy

1. A de novo frameshift mutation in chromodomain helicase DNA‐binding domain 8 (CHD8): A case report and literature review. Issue 5 (20th January 2016)

Authors:
Merner, Nancy; Forgeot d'Arc, Baudouin; Bell, Scott C.; Maussion, Gilles; Peng, Huashan; Gauthier, Julie; Crapper, Liam; Hamdan, Fadi F.; Michaud, Jacques L.; Mottron, Laurent; Rouleau, Guy A.; Ernst, Carl
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 5(2016)
Page Start:
1225
Record Type:
Journal Article
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2. A Novel Deletion in SMPX Causes a Rare form of X‐Linked Progressive Hearing Loss in Two Families Due to a Founder Effect. Issue 1 (11th October 2012)

Authors:
Abdelfatah, Nelly; Merner, Nancy; Houston, Jim; Benteau, Tammy; Griffin, Anne; Doucette, Lance; Stockley, Tracy; Lauzon, Julie L.; Young, Terry‐Lynn
Journal:
Human mutation
Issue:
Volume 34:Issue 1(2013:Jan.)
Page Start:
66
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗