@article{Black_2021,<br/><span class="tab"></span> title={The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement},<br/><span class="tab"></span> volume={16},<br/><span class="tab"></span> ISSN={1750-1172},<br/><span class="tab"></span> url={http://dx.doi.org/10.1186/s13023-021-01756-x},<br/><span class="tab"></span> DOI={10.1186/s13023-021-01756-x},<br/><span class="tab"></span> number={1},<br/><span class="tab"></span> journal={Orphanet Journal of Rare Diseases},<br/><span class="tab"></span> publisher={Springer Science and Business Media LLC},<br/><span class="tab"></span> author={Black,<br/><span class="tab"></span> Graeme C. and Sergouniotis,<br/><span class="tab"></span> Panagiotis and Sodi,<br/><span class="tab"></span> Andrea and Leroy,<br/><span class="tab"></span> Bart P. and Van Cauwenbergh,<br/><span class="tab"></span> Caroline and Liskova,<br/><span class="tab"></span> Petra and Grønskov,<br/><span class="tab"></span> Karen and Klett,<br/><span class="tab"></span> Artur and Kohl,<br/><span class="tab"></span> Susanne and Taurina,<br/><span class="tab"></span> Gita and Sukys,<br/><span class="tab"></span> Marius and Haer-Wigman,<br/><span class="tab"></span> Lonneke and Nowomiejska,<br/><span class="tab"></span> Katarzyna and Marques,<br/><span class="tab"></span> João Pedro and Leroux,<br/><span class="tab"></span> Dorothée and Cremers,<br/><span class="tab"></span> Frans P. M. and De Baere,<br/><span class="tab"></span> Elfride and Dollfus,<br/><span class="tab"></span> Hélène},<br/><span class="tab"></span> year={2021},<br/><span class="tab"></span> month=mar }