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Author/Creator Stavropoulos, Dimitri

1. Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity. (November 2018)

Authors:
Selvanayagam, Thanuja; Walker, Susan; Gazzellone, Matthew; Kellam, Barbara; Cytrynbaum, Cheryl; Stavropoulos, Dimitri; Li, Ping; Birken, Catherine; Hamilton, Jill; Weksberg, Rosanna; Scherer, Stephen
Journal:
European journal of human genetics
Issue:
Volume 26:Number 11(2018)
Page Start:
1588
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. (December 2015)

Authors:
Marshall, Christian; Farrell, Sandra; Cushing, Donna; Paton, Tara; Stockley, Tracy; Stavropoulos, Dimitri; Ray, Peter; Szego, Michael; Lau, Lynette; Pereira, Sergio; Cohn, Ronald; Wintle, Richard; Abuzenadah, Adel; Abu-Elmagd, Muhammad; Scherer, Stephen
Journal:
BMC genomics
Issue:
Volume 16:Number 1(2015)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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