Search

Author/Creator Dimopoulos, Aggeliki

2. Copy number variants in a population‐based investigation of Klippel–Trenaunay syndrome. Issue 2 (30th November 2016)

Authors:
Dimopoulos, Aggeliki; Sicko, Robert J.; Kay, Denise M.; Rigler, Shannon L.; Fan, Ruzong; Romitti, Paul A.; Browne, Marilyn L.; Druschel, Charlotte M.; Caggana, Michele; Brody, Lawrence C.; Mills, James L.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 2(2017)
Page Start:
352
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease. Issue 8 (August 2017)

Authors:
Hernández-Ramírez, Laura C; Gam, Ryhem; Valdés, Nuria; Lodish, Maya B; Pankratz, Nathan; Balsalobre, Aurelio; Gauthier, Yves; Faucz, Fabio R; Trivellin, Giampaolo; Chittiboina, Prashant; Lane, John; Kay, Denise M; Dimopoulos, Aggeliki; Gaillard, Stephan; Neou, Mario; Bertherat, Jérôme; Assié, Gui...
Journal:
Endocrine-related cancer
Issue:
Volume 24:Issue 8(2017)
Page Start:
379
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Rare copy number variants in a population‐based investigation of hypoplastic right heart syndrome. Issue 1 (20th January 2017)

Authors:
Dimopoulos, Aggeliki; Sicko, Robert J.; Kay, Denise M.; Rigler, Shannon L.; Druschel, Charlotte M.; Caggana, Michele; Browne, Marilyn L.; Fan, Ruzong; Romitti, Paul A.; Brody, Lawrence C.; Mills, James L.
Journal:
Birth defects research
Issue:
Volume 109:Issue 1(2017)
Page Start:
8
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗