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Author/Creator Place, Emily M.

1. Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome. (4th March 2023)

Authors:
Hoyek, Sandra; Wang, Marlene; Berrocal, Audina M.; Wong, Ashley; Place, Emily M.; Mason-Suares, Heather; Lin, Angela E.; Mukai, Shizuo; Patel, Nimesh A.
Journal:
Ophthalmic genetics
Issue:
Volume 44:Number 2(2023)
Page Start:
198
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. (4th May 2022)

Authors:
Catomeris, Andrew J.; Ballios, Brian G.; Sangermano, Riccardo; Wagner, Naomi E.; Comander, Jason I.; Pierce, Eric A.; Place, Emily M.; Bujakowska, Kinga M.; Huckfeldt, Rachel M.
Journal:
Ophthalmic genetics
Issue:
Volume 43:Number 3(2022)
Page Start:
332
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗