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Results by year

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

Year Number of Results
1982 1
1983 2
1984 2
1985 2
1986 1
1987 1
1988 2
1990 2
1991 1
1994 2
1997 1
1998 2
1999 2
2000 4
2001 3
2002 2
2003 3
2004 7
2005 4
2006 6
2007 8
2008 5
2009 2
2010 4
2011 9
2012 7
2013 4
2014 5
2015 5
2017 5
2018 5
2019 7
2020 2
2021 4
2022 2
2024 0

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Similar articles for PMID: 22077972

106 results

Results by year

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Page 1
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Weber S, Thiele H, Mir S, Toliat MR, Sozeri B, Reutter H, Draaken M, Ludwig M, Altmüller J, Frommolt P, Stuart HM, Ranjzad P, Hanley NA, Jennings R, Newman WG, Wilcox DT, Thiel U, Schlingmann KP, Beetz R, Hoyer PF, Konrad M, Schaefer F, Nürnberg P, Woolf AS. Weber S, et al. Am J Hum Genet. 2011 Nov 11;89(5):668-74. doi: 10.1016/j.ajhg.2011.10.007. Am J Hum Genet. 2011. PMID: 22077972 Free PMC article.
Genetics of human congenital urinary bladder disease.
Woolf AS, Stuart HM, Newman WG. Woolf AS, et al. Pediatr Nephrol. 2014 Mar;29(3):353-60. doi: 10.1007/s00467-013-2472-1. Epub 2013 Apr 13. Pediatr Nephrol. 2014. PMID: 23584850 Review.
106 results