Retinal morphology in patients with BBS1 and BBS10 related Bardet–Biedl Syndrome evaluated by Fourier-domain optical coherence tomography-Reference-Cited by-同舟云学术

Retinal morphology in patients with BBS1 and BBS10 related Bardet–Biedl Syndrome evaluated by Fourier-domain optical coherence tomography

Published:2008-02 Issue:3 Volume:48 Page:392-399
ISSN:0042-6989
Container-title:Vision Research
language:en
Short-container-title:Vision Research

Author:

Gerth Christina,Zawadzki Robert J.,Werner John S.,Héon Elise

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference31 articles.

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4. Retinal disease expression in Bardet–Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degeneration;Azari;Investigative Ophthalmology & Visual Science,2006

5. Sur un syndrome d’obésité congénitale avec polydactylie et réunite pigmentaire (contribution á l’etude des formes cliniques de l’obésite hypophysaire);Bardet;Thése de Paris,1920

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2. Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants;American Journal of Medical Genetics Part A;2023-06-09

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4. Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation Sequencing;International Journal of Molecular Sciences;2022-01-17

5. Bardet-Biedl-Syndrom – Diagnose und klinischer Verlauf;Klinische Monatsblätter für Augenheilkunde;2020-03