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Author/Creator Levin, Alex V

2. Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. Issue 17 (27th May 2021)

Authors:
Reis, Linda M; Sorokina, Elena A; Dudakova, Lubica; Moravikova, Jana; Skalicka, Pavlina; Malinka, Frantisek; Seese, Sarah E; Thompson, Samuel; Bardakjian, Tanya; Capasso, Jenina; Allen, William; Glaser, Tom; Levin, Alex V; Schneider, Adele; Khan, Ayesha; Liskova, Petra; Semina, Elena V
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 17(2021)
Page Start:
1591
Record Type:
Journal Article
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7. The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. Issue 4 (21st November 2010)

Authors:
Robitaille, Johane M; Zheng, Binyou; Wallace, Karin; Beis, M Jill; Tatlidil, Cuneyt; Yang, Jenny; Sheidow, Tom G; Siebert, Lee; Levin, Alex V; Lam, Wai-Ching; Arthur, Brian W; Lyons, Christopher J; Jaakkola, Elisa; Tsilou, Ekaterini; Williams, Charles A; Weaver, Richard Grey; Shields, Carol L; Gu...
Journal:
British journal of ophthalmology
Issue:
Volume 95:Issue 4(2011)
Page Start:
574
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. Use of the Delphi process in paediatric cataract management. Issue 5 (29th September 2015)

Authors:
Serafino, Massimiliano; Trivedi, Rupal H; Levin, Alex V; Wilson, M Edward; Nucci, Paolo; Lambert, Scott R; Nischal, Ken K; Plager, David A; Bremond-Gignac, Dominique; Kekunnaya, Ramesh; Nishina, Sachiko; Tehrani, Nasrin N; Ventura, Marcelo C
Journal:
British journal of ophthalmology
Issue:
Volume 100:Issue 5(2016)
Page Start:
611
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗