Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1936 1
1952 1
1954 1
1958 7
1959 1
1960 1
1961 2
1962 2
1963 1
1966 1
1967 1
1968 1
1971 1
1973 1
1975 1
1978 2
1979 1
1980 3
1982 4
1983 1
1984 2
1986 1
1987 2
1992 2
1993 3
1994 1
1995 4
1996 2
1998 4
1999 4
2000 1
2001 6
2002 13
2003 10
2004 6
2005 19
2006 19
2007 19
2008 20
2009 29
2010 16
2011 23
2012 22
2013 7
2014 15
2015 13
2016 10
2017 7
2018 5
2019 8
2020 13
2021 4
Text availability
Article attribute
Article type
Publication date

Similar articles for PMID: 17088400

308 results
Results by year
Filters applied: . Clear all
Page 1
Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.
Lugtenberg D, Kleefstra T, Oudakker AR, Nillesen WM, Yntema HG, Tzschach A, Raynaud M, Rating D, Journel H, Chelly J, Goizet C, Lacombe D, Pedespan JM, Echenne B, Tariverdian G, O'Rourke D, King MD, Green A, van Kogelenberg M, Van Esch H, Gecz J, Hamel BC, van Bokhoven H, de Brouwer AP. Lugtenberg D, et al. Eur J Hum Genet. 2009 Apr;17(4):444-53. doi: 10.1038/ejhg.2008.208. Epub 2008 Nov 5. Eur J Hum Genet. 2009. PMID: 18985075 Free PMC article.
Neurologic aspects of MECP2 gene duplication in male patients.
Echenne B, Roubertie A, Lugtenberg D, Kleefstra T, Hamel BC, Van Bokhoven H, Lacombe D, Philippe C, Jonveaux P, de Brouwer AP. Echenne B, et al. Pediatr Neurol. 2009 Sep;41(3):187-91. doi: 10.1016/j.pediatrneurol.2009.03.012. Pediatr Neurol. 2009. PMID: 19664534
308 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page