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

Year Number of Results
1958 1
1962 1
1977 1
1979 1
1984 1
1989 1
1990 1
1992 2
1993 6
1994 1
1996 1
1997 1
1998 2
1999 1
2000 1
2003 1
2005 3
2007 5
2008 2
2009 4
2010 7
2011 4
2012 4
2013 5
2014 11
2015 7
2016 7
2017 6
2018 6
2019 4
2020 13
2021 13
2022 7
2023 3
2024 0

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Similar articles for PMID: 27187611

121 results

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Page 1
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome.
Hildebrandt CC, Patel N, Graham JM Jr, Bamshad M, Nickerson DA, White JJ, Marvin CT, Miller DE; University of Washington Center for Mendelian Genomics; Grand KL, Sanchez-Lara PA, Schweitzer D, Al-Zaidan HI, Al Masseri Z, Alkuraya FS, Lin AE. Hildebrandt CC, et al. Am J Med Genet A. 2021 Jul;185(7):2136-2149. doi: 10.1002/ajmg.a.62194. Epub 2021 Mar 30. Am J Med Genet A. 2021. PMID: 33783941
FAM20C Overview: Classic and Novel Targets, Pathogenic Variants and Raine Syndrome Phenotypes.
Palma-Lara I, Pérez-Ramírez M, García Alonso-Themann P, Espinosa-García AM, Godinez-Aguilar R, Bonilla-Delgado J, López-Ornelas A, Victoria-Acosta G, Olguín-García MG, Moreno J, Palacios-Reyes C. Palma-Lara I, et al. Int J Mol Sci. 2021 Jul 27;22(15):8039. doi: 10.3390/ijms22158039. Int J Mol Sci. 2021. PMID: 34360805 Free PMC article. Review.
121 results