Browsing Universitätsbibliographie by Author "Sliesoraityte, Ieva"

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A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect

Kohl, Susanne; Llavona, Pablo; Sauer, Alexandra; Reuter, Peggy; Weisschuh, Nicole; Kempf, Melanie; Dehmelt, Florian Alexander; Arrenberg, Aristides B.; Sliesoraityte, Ieva; Zrenner, Eberhart; van Schooneveld, Mary J.; Rudolph, Gunther; Kuhlewein, Laura; Wissinger, Bernd (2021)
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Bonnet, Crystel; Riahi, Zied; Chantot-Bastaraud, Sandra; Smagghe, Luce; Letexier, Melanie; Marcaillou, Charles; Lefevre, Gaelle M.; Hardelin, Jean-Pierre; El-Amraoui, Aziz; Singh-Estivalet, Amrit; Mohand-Said, Saddek; Kohl, Susanne; Kurtenbach, Anne; Sliesoraityte, Ieva; Zobor, Ditta; Gherbi, Souad; Testa, Francesco; Simonelli, Francesca; Banfi, Sandro; Fakin, Ana; Glavac, Damjan; Jarc-Vidmar, Martina; Zupan, Andrej; Battelino, Saba; Martorell Sampol, Loreto; Antonia Claveria, Maria; Catala Mora, Jaume; Dad, Shzeena; Moller, Lisbeth B.; Rodriguez Jorge, Jesus; Hawlina, Marko; Auricchio, Alberto; Sahel, Jose-Alain; Marlin, Sandrine; Zrenner, Eberhart; Audo, Isabelle; Petit, Christine (2016)
BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome

Estrada-Cuzcano, Alejandro; Koenekoop, Robert K.; Senechal, Audrey; De Baere, Elfride B. W.; de Ravel, Thomy; Banfi, Sandro; Kohl, Susanne; Ayuso, Carmen; Sharon, Dror; Hoyng, Carel B.; Hamel, Christian P.; Leroy, Bart P.; Ziviello, Carmela; Lopez, Irma; Bazinet, Alexandre; Wissinger, Bernd; Sliesoraityte, Ieva; Avila-Fernandez, Almudena; Littink, Karin W.; Vingolo, Enzo M.; Signorini, Sabrina; Banin, Eyal; Mizrahi-Meissonnier, Liliana; Zrenner, Eberhard; Kellner, Ulrich; Collin, Rob W. J.; den Hollander, Anneke I.; Cremers, Frans P. M.; Klevering, Jeroen (2012)
Correlation Between Spectral Domain OCT Retinal Nerve Fibre Layer Thickness and Multifocal Pattern Electroretinogram in Advanced Retinitis Pigmentosa

Sliesoraityte, Ieva; Troeger, Eric; Bernd, Antje; Kurtenbach, Anne; Zrenner, Eberhart (2012)
Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German Cohort

Zobor, Ditta; Zobor, Gergely; Hipp, Stephanie; Baumann, Britta; Weisschuh, Nicole; Biskup, Saskia; Sliesoraityte, Ieva; Zrenner, Eberhart; Kohl, Susanne (2018)

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