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Results by year

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

Year Number of Results
1993 1
1999 3
2002 1
2003 3
2004 1
2005 1
2006 2
2007 3
2008 1
2010 1
2011 1
2013 1
2014 3
2015 1
2019 1
2020 1
2021 1
2022 1
2023 0

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PubMed for id: 346973

24 results

Results by year

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Page 1
Long-term follow-up in patients with CCFDN syndrome.
Walter MC, Bernert G, Zimmermann U, Müllner-Eidenböck A, Moser E, Kalaydjieva L, Lochmüller H, Müller-Felber W. Walter MC, et al. Neurology. 2014 Oct 7;83(15):1337-44. doi: 10.1212/WNL.0000000000000874. Epub 2014 Sep 3. Neurology. 2014. PMID: 25186864
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome.
Varon R, Gooding R, Steglich C, Marns L, Tang H, Angelicheva D, Yong KK, Ambrugger P, Reinhold A, Morar B, Baas F, Kwa M, Tournev I, Guerguelcheva V, Kremensky I, Lochmüller H, Müllner-Eidenböck A, Merlini L, Neumann L, Bürger J, Walter M, Swoboda K, Thomas PK, von Moers A, Risch N, Kalaydjieva L. Varon R, et al. Nat Genet. 2003 Oct;35(2):185-9. doi: 10.1038/ng1243. Epub 2003 Sep 21. Nat Genet. 2003. PMID: 14517542
24 results