Novel variant in FGFR2 in a family with anterior segment anomalies.

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Bibliographic Details
Title: Novel variant in FGFR2 in a family with anterior segment anomalies.
Authors: Chattannavar G; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, University of Rochester, Rochester, New York, USA.; Jasti V Ramanamma Children's Eye Care Centre, Child Sight Institute, L V Prasad Eye Institute, Hyderabad, India., Haefeli LM; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, University of Rochester, Rochester, New York, USA.; The University of Iowa Institute for Vision Research and the Department of Ophthalmology and Visual Sciences, Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA., Procopio R; Pediatric Ophthalmology & Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA., Reis LM; Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA., Capasso JE; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, University of Rochester, Rochester, New York, USA.; Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, New York, USA., Thuma TBT; Pediatric Ophthalmology & Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA., Semina EV; Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA., Schneider A; Pediatric Ophthalmology & Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA., Levin AV; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, University of Rochester, Rochester, New York, USA.; Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, New York, USA.
Source: Ophthalmic genetics [Ophthalmic Genet] 2026 Jun; Vol. 47 (3), pp. 304-308. Date of Electronic Publication: 2026 Jan 04.
Publication Type: Journal Article; Case Reports; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1744-5094
DOI:10.1080/13816810.2025.2611116