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

Year Number of Results
1989 2
1990 1
1991 1
1992 2
1993 7
1994 3
1995 8
1996 5
1997 3
1998 14
1999 5
2000 9
2001 8
2002 9
2003 6
2004 7
2005 9
2006 9
2007 15
2008 12
2009 17
2010 17
2011 6
2012 11
2013 14
2014 6
2015 2
2016 2
2024 0

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196 results

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Page 1
The skeletal dysplasias.
Krakow D, Rimoin DL. Krakow D, et al. Genet Med. 2010 Jun;12(6):327-41. doi: 10.1097/GIM.0b013e3181daae9b. Genet Med. 2010. PMID: 20556869 Free article. Review.
Sulfate transport in chondrodysplasia.
Hästbacka J, Superti-Furga A, Wilcox WR, Rimoin DL, Cohn DH, Lander ES. Hästbacka J, et al. Ann N Y Acad Sci. 1996 Jun 8;785:131-6. doi: 10.1111/j.1749-6632.1996.tb56251.x. Ann N Y Acad Sci. 1996. PMID: 8702119 Review. No abstract available.
Signaling pathways in human skeletal dysplasias.
Baldridge D, Shchelochkov O, Kelley B, Lee B. Baldridge D, et al. Annu Rev Genomics Hum Genet. 2010;11:189-217. doi: 10.1146/annurev-genom-082908-150158. Annu Rev Genomics Hum Genet. 2010. PMID: 20690819 Review.
MICRO syndrome: an entity distinct from COFS syndrome.
Graham JM Jr, Hennekam R, Dobyns WB, Roeder E, Busch D. Graham JM Jr, et al. Am J Med Genet A. 2004 Jul 30;128A(3):235-45. doi: 10.1002/ajmg.a.30060. Am J Med Genet A. 2004. PMID: 15216543 Review.
Gracile bone dysplasia.
Thomas JA, Rimoin DL, Lachman RS, Wilcox WR. Thomas JA, et al. Am J Med Genet. 1998 Jan 6;75(1):95-100. Am J Med Genet. 1998. PMID: 9450865
196 results