DICER1 Syndrome: Characterization of the Ocular Phenotype in a Family-Based Cohort Study.

Authors

Laryssa A. Huryn
Amy Turriff
Laura A. Harney
Ann Garrity Carr
Patricia Chevez-Barrios
Dan S. Gombos
Radha Ram
Robert B. Hufnagel
D Ashley Hill, George Washington University
Wadih M. Zein
Kris Ann P Schultz
Rachel Bishop
Douglas R. Stewart

Document Type

Journal Article

Publication Date

2-1-2019

Journal

Ophthalmology

Volume

126

Issue

2

Inclusive Pages

296-304

DOI

10.1016/j.ophtha.2018.09.038

Keywords

Adolescent; Adult; Aged; Case-Control Studies; Child; Child, Preschool; Ciliary Body; DEAD-box RNA Helicases; DNA, Neoplasm; Electroretinography; Female; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Humans; Infant; Male; Middle Aged; Neuroectodermal Tumors, Primitive; Phenotype; Prospective Studies; Retinal Pigment Epithelium; Ribonuclease III; Slit Lamp Microscopy; Syndrome; Tomography, Optical Coherence; Uveal Neoplasms; Visual Acuity; Young Adult

Comments

Epub 2018 Oct 17

APA Citation

Huryn, L. A., Turriff, A., Harney, L. A., Carr, A. G., Chevez-Barrios, P., Gombos, D. S., Ram, R., Hufnagel, R. B., Hill, D., Zein, W. M., Schultz, K. A., Bishop, R., & Stewart, D. R. (2019). DICER1 Syndrome: Characterization of the Ocular Phenotype in a Family-Based Cohort Study.. Ophthalmology, 126 (2). http://dx.doi.org/10.1016/j.ophtha.2018.09.038

Peer Reviewed

1