1. Congenital Microphthalmia, Anophthalmia and Coloboma among Live Births in Denmark. (2nd September 2016) Authors: Roos, Laura; Jensen, Hanne; Grønskov, Karen; Holst, René; Tümer, Zeynep Journal: Ophthalmic epidemiology Issue: Volume 23:Number 5(2016) Page Start: 324 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Epidemiology of ectopia lentis and outcomes after surgery in a Danish population. Issue 12 (December 2022) Authors: Rasul, Asrin; Roos, Laura; Groth, Kristian; Riise, Per; Bach-Holm, Daniella; Kessel, Line Journal: Journal of cataract and refractive surgery Issue: Volume 48:Issue 12(2022) Page Start: 1394 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA gene. Issue 3 (July 2017) Authors: Bayat, Allan; Kirchhoff, Maria; Madsen, Camilla G.; Roos, Laura; Kreiborg, Sven Journal: Clinical dysmorphology Issue: Volume 26:Issue 3(2017:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic disease is a common cause of bilateral childhood cataract in Denmark. (2nd November 2021) Authors: Kessel, Line; Bach-Holm, Daniella; Al-Bakri, Moug; Roos, Laura; Lund, Allan; Grønskov, Karen Journal: Ophthalmic genetics Issue: Volume 42:Number 6(2021) Page Start: 650 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Preimplantation genetic testing in two Danish couples affected by Peutz–Jeghers syndrome. (4th March 2023) Authors: Byrjalsen, Anna; Roos, Laura; Diemer, Tue; Karstensen, John Gásdal; Løssl, Kristine; Jelsig, Anne Marie Journal: Scandinavian journal of gastroenterology Issue: Volume 58:Number 3(2023) Page Start: 314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prevalence and causes of infantile nystagmus in a large population‐based Danish cohort. Issue 5 (17th February 2020) Authors: Hvid, Karen; Nissen, Kamilla Rothe; Bayat, Allan; Roos, Laura; Grønskov, Karen; Kessel, Line Journal: Acta ophthalmologica Issue: Volume 98:Issue 5(2020) Page Start: 506 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Refinement of genotype‐phenotype correlation in 18 patients carrying a 1q24q25 deletion. (25th February 2015) Authors: Chatron, Nicolas; Haddad, Véronique; Andrieux, Joris; Désir, Julie; Boute, Odile; Dieux, Anne; Baumann, Clarisse; Drunat, Séverine; Gérard, Marion; Bonnet, Céline; Leheup, Bruno; Till, Marianne; Rossi, Massimiliano; Flori, Elisabeth; Alembik, Yves; Stewart, Helen; McParland, Joanna; Bernardini, L... Journal: American journal of medical genetics Issue: Volume 167:Number 5(2015:May) Page Start: 1008 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes. Issue 8 (27th June 2013) Authors: Curry, Cynthia J.; Rosenfeld, Jill A.; Grant, Erica; Gripp, Karen W.; Anderson, Carol; Aylsworth, Arthur S.; Saad, Taha Ben; Chizhikov, Victor V.; Dybose, Giedre; Fagerberg, Christina; Falco, Michelle; Fels, Christina; Fichera, Marco; Graakjaer, Jesper; Greco, Donatella; Hair, Jennifer; Hopkins, ... Journal: American journal of medical genetics Issue: Volume 161:Issue 8(2013:Aug.) Page Start: 1833 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗