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Results by year

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

Year Number of Results
1983 1
1991 1
1992 1
1993 2
1994 1
1995 3
1996 2
1997 1
1998 3
1999 3
2000 4
2001 2
2002 4
2003 3
2004 6
2005 7
2006 6
2007 3
2008 2
2009 7
2010 7
2011 4
2012 4
2013 6
2014 3
2015 4
2016 6
2017 2
2018 1
2020 2
2021 1
2022 1
2024 0

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Similar articles for PMID: 12070251

93 results

Results by year

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Page 1
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations.
Petrij F, Dauwerse HG, Blough RI, Giles RH, van der Smagt JJ, Wallerstein R, Maaswinkel-Mooy PD, van Karnebeek CD, van Ommen GJ, van Haeringen A, Rubinstein JH, Saal HM, Hennekam RC, Peters DJ, Breuning MH. Petrij F, et al. J Med Genet. 2000 Mar;37(3):168-76. doi: 10.1136/jmg.37.3.168. J Med Genet. 2000. PMID: 10699051 Free PMC article.
[Rubinstein-Taybi syndrome].
Tsukahara M, Tsujino K. Tsukahara M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):241-3. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057213 Review. Japanese. No abstract available.
New CBP mutations in Brazilian patients with Rubinstein-Taybi syndrome.
Suzuki KT, Torres LC, Sugayama SM, Aguiar Alves Bda C, Moreira-Filho CA, Carneiro-Sampaio M. Suzuki KT, et al. Clin Genet. 2013 Mar;83(3):291-2. doi: 10.1111/j.1399-0004.2012.01894.x. Epub 2012 May 17. Clin Genet. 2013. PMID: 22591219 No abstract available.
93 results