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Causes of poor eye contact in infants: a population-based study.
Levinsen M, Børresen ML, Roos L, Grønskov K, Kessel L. Levinsen M, et al. Among authors: roos l. BMC Ophthalmol. 2021 Nov 7;21(1):388. doi: 10.1186/s12886-021-02151-7. BMC Ophthalmol. 2021. PMID: 34743689 Free PMC article.
The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.
Black GC, Sergouniotis P, Sodi A, Leroy BP, Van Cauwenbergh C, Liskova P, Grønskov K, Klett A, Kohl S, Taurina G, Sukys M, Haer-Wigman L, Nowomiejska K, Marques JP, Leroux D, Cremers FPM, De Baere E, Dollfus H; ERN-EYE study group. Black GC, et al. Orphanet J Rare Dis. 2021 Mar 20;16(1):142. doi: 10.1186/s13023-021-01756-x. Orphanet J Rare Dis. 2021. PMID: 33743793 Free PMC article.
Is MED13L-related intellectual disability a recognizable syndrome?
Tørring PM, Larsen MJ, Brasch-Andersen C, Krogh LN, Kibæk M, Laulund L, Illum N, Dunkhase-Heinl U, Wiesener A, Popp B, Marangi G, Hjortshøj TD, Ek J, Vogel I, Becher N, Roos L, Zollino M, Fagerberg CR. Tørring PM, et al. Among authors: roos l. Eur J Med Genet. 2019 Feb;62(2):129-136. doi: 10.1016/j.ejmg.2018.06.014. Epub 2018 Jun 27. Eur J Med Genet. 2019. PMID: 29959045
[Genetic screening of prospective parents].
Smed VM, Petersen OBB, Gerdes AA, Diness BR, Roos LS. Smed VM, et al. Ugeskr Laeger. 2021 Mar 29;183(13):V12200933. Ugeskr Laeger. 2021. PMID: 33829993 Free article. Review. Danish.
765 results