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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1981 1
1983 3
1988 1
1990 3
1991 4
1992 9
1993 7
1994 3
1995 7
1996 5
1997 14
1998 8
1999 9
2000 11
2001 8
2002 5
2003 4
2004 6
2005 10
2006 9
2007 5
2008 8
2009 8
2010 5
2011 13
2012 6
2013 7
2014 10
2015 7
2016 3
2018 7
2019 6
2020 3
2021 1
2022 1
2024 1

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206 results

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Page 1
Cornelia de Lange syndrome.
Boyle MI, Jespersgaard C, Brøndum-Nielsen K, Bisgaard AM, Tümer Z. Boyle MI, et al. Among authors: brondum nielsen k. Clin Genet. 2015 Jul;88(1):1-12. doi: 10.1111/cge.12499. Epub 2014 Oct 28. Clin Genet. 2015. PMID: 25209348 Review.
Oculocutaneous albinism.
Grønskov K, Ek J, Brondum-Nielsen K. Grønskov K, et al. Among authors: brondum nielsen k. Orphanet J Rare Dis. 2007 Nov 2;2:43. doi: 10.1186/1750-1172-2-43. Orphanet J Rare Dis. 2007. PMID: 17980020 Free PMC article. Review.
[Marriages between cousins].
Brøndum-Nielsen K. Brøndum-Nielsen K. Ugeskr Laeger. 2003 Apr 28;165(18):1849. Ugeskr Laeger. 2003. PMID: 12772390 Danish. No abstract available.
Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature.
Schönewolf-Greulich B, Bisgaard AM, Møller RS, Dunø M, Brøndum-Nielsen K, Kaur S, Van Bergen NJ, Lunke S, Eggers S, Jespersgaard C, Christodoulou J, Tümer Z. Schönewolf-Greulich B, et al. Among authors: brondum nielsen k. Clin Genet. 2019 Feb;95(2):221-230. doi: 10.1111/cge.13153. Epub 2018 Jan 25. Clin Genet. 2019. PMID: 29023665 Review.
[The genome in terms of audiology and ophthalmology].
Tranebjærg L, Rendtorff ND, Brøndum-Nielsen K. Tranebjærg L, et al. Among authors: brondum nielsen k. Ugeskr Laeger. 2014 Nov 10;176(46):V06140365. Ugeskr Laeger. 2014. PMID: 25394931 Free article. Review. Danish.
Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements.
Schönewolf-Greulich B, Bisgaard AM, Dunø M, Jespersgaard C, Rokkjaer M, Hansen LK, Tsoutsou E, Sofokleous C, Topcu M, Kaur S, Van Bergen NJ, Brøndum-Nielsen K, Larsen MJ, Sørensen KP, Christodoulou J, Fagerberg CR, Tümer Z. Schönewolf-Greulich B, et al. Among authors: brondum nielsen k. Clin Genet. 2019 Mar;95(3):403-408. doi: 10.1111/cge.13473. Epub 2018 Dec 7. Clin Genet. 2019. PMID: 30417326 Review.
206 results