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

Year Number of Results
1976 1
1982 1
1985 1
1987 1
1988 2
1989 5
1990 2
1991 7
1992 1
1993 1
1994 1
1995 1
1996 3
1997 2
1998 2
1999 3
2000 4
2001 5
2002 2
2003 3
2004 2
2005 1
2006 3
2007 4
2008 6
2009 5
2012 2
2013 4
2014 4
2015 8
2016 2
2017 5
2018 4
2019 6
2021 1
2022 3
2023 1
2024 0

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Similar articles for PMID: 9801784

99 results

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Page 1
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype.
Terhal PA, Nievelstein RJ, Verver EJ, Topsakal V, van Dommelen P, Hoornaert K, Le Merrer M, Zankl A, Simon ME, Smithson SF, Marcelis C, Kerr B, Clayton-Smith J, Kinning E, Mansour S, Elmslie F, Goodwin L, van der Hout AH, Veenstra-Knol HE, Herkert JC, Lund AM, Hennekam RC, Mégarbané A, Lees MM, Wilson LC, Male A, Hurst J, Alanay Y, Annerén G, Betz RC, Bongers EM, Cormier-Daire V, Dieux A, David A, Elting MW, van den Ende J, Green A, van Hagen JM, Hertel NT, Holder-Espinasse M, den Hollander N, Homfray T, Hove HD, Price S, Raas-Rothschild A, Rohrbach M, Schroeter B, Suri M, Thompson EM, Tobias ES, Toutain A, Vreeburg M, Wakeling E, Knoers NV, Coucke P, Mortier GR. Terhal PA, et al. Am J Med Genet A. 2015 Mar;167A(3):461-75. doi: 10.1002/ajmg.a.36922. Epub 2015 Jan 21. Am J Med Genet A. 2015. PMID: 25604898
A case report of spondyloepiphyseal dysplasia congenita.
Gembun Y, Nakayama Y, Shirai Y, Miyamoto M, Sawaizumi T, Kitamura S. Gembun Y, et al. J Nippon Med Sch. 2001 Apr;68(2):186-9. doi: 10.1272/jnms.68.186. J Nippon Med Sch. 2001. PMID: 11301365 Free article. Review.
99 results