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

Year Number of Results
1959 2
1990 1
1998 2
1999 2
2000 5
2001 7
2002 3
2003 3
2004 6
2005 10
2006 4
2007 8
2008 3
2009 2
2010 5
2011 4
2012 4
2014 1
2015 3
2024 0

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PubMed (Bookshelf cited) for id: 325376

68 results

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Page 1
New therapeutic targets in rare genetic skeletal diseases.
Briggs MD, Bell PA, Wright MJ, Pirog KA. Briggs MD, et al. Expert Opin Orphan Drugs. 2015 Oct 3;3(10):1137-1154. doi: 10.1517/21678707.2015.1083853. Epub 2015 Sep 24. Expert Opin Orphan Drugs. 2015. PMID: 26635999 Free PMC article.
Nosology and classification of genetic skeletal disorders: 2015 revision.
Bonafe L, Cormier-Daire V, Hall C, Lachman R, Mortier G, Mundlos S, Nishimura G, Sangiorgi L, Savarirayan R, Sillence D, Spranger J, Superti-Furga A, Warman M, Unger S. Bonafe L, et al. Am J Med Genet A. 2015 Dec;167A(12):2869-92. doi: 10.1002/ajmg.a.37365. Epub 2015 Sep 23. Am J Med Genet A. 2015. PMID: 26394607
A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study.
Zhao J, Xia W, Nie M, Zheng X, Wang Q, Wang X, Wang W, Ning Z, Huang W, Jiang Y, Li M, Wang O, Xing X, Sun Y, Luo L, He S, Yu W, Lin Q, Pei Y, Zhang F, Han Y, Tong Y, Che Y, Shen R, Hu Y, Zhou X, Chen Q, Xu L. Zhao J, et al. Bone. 2012 Apr;50(4):917-24. doi: 10.1016/j.bone.2012.01.003. Epub 2012 Jan 16. Bone. 2012. PMID: 22270056 Free PMC article.
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes.
Kim OH, Park H, Seong MW, Cho TJ, Nishimura G, Superti-Furga A, Unger S, Ikegawa S, Choi IH, Song HR, Kim HW, Yoo WJ, Shim JS, Chung CY, Oh CW, Jeong C, Song KS, Seo SG, Cho SI, Yeo IK, Kim SY, Park S, Park SS. Kim OH, et al. Am J Med Genet A. 2011 Nov;155A(11):2669-80. doi: 10.1002/ajmg.a.34246. Epub 2011 Sep 30. Am J Med Genet A. 2011. PMID: 21965141
Pseudoachondroplasia and multiple epiphyseal dysplasia: a 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution.
Jackson GC, Mittaz-Crettol L, Taylor JA, Mortier GR, Spranger J, Zabel B, Le Merrer M, Cormier-Daire V, Hall CM, Offiah A, Wright MJ, Savarirayan R, Nishimura G, Ramsden SC, Elles R, Bonafe L, Superti-Furga A, Unger S, Zankl A, Briggs MD. Jackson GC, et al. Hum Mutat. 2012 Jan;33(1):144-57. doi: 10.1002/humu.21611. Epub 2011 Oct 31. Hum Mutat. 2012. PMID: 21922596 Free PMC article.
68 results