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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 4
2011 11
2012 6
2013 7
2014 10
2015 7
2016 3
2018 7
2019 6
2020 3
2021 1
2022 1
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Article attribute
Article type
Publication date

Search Results

202 results
Results by year
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Page 1
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.
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.
[Clinical molecular genetics diagnostics of Rett syndrome in Denmark].
Schönewolf-Greulich B, Dunø M, Ravn K, Brøndum-Nielsen K, Bisgaard AM. Schönewolf-Greulich B, et al. Among authors: brondum nielsen k. Ugeskr Laeger. 2015 Jun 29;177(27):V12140731. Ugeskr Laeger. 2015. PMID: 26239739 Free article. Review. Danish.
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.
202 results