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

Year Number of Results
1965 1
1990 1
1992 3
1993 2
1994 5
1995 2
1996 2
1997 3
1998 4
1999 4
2000 6
2001 6
2002 2
2003 2
2004 5
2005 1
2006 1
2007 1
2008 4
2009 1
2010 1
2011 3
2012 3
2013 2
2014 1
2019 1
2024 0

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63 results

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Page 1
Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutations.
Van-Gils J, Naudion S, Toutain J, Lancelot G, Attié-Bitach T, Blesson S, Demeer B, Doray B, Gonzales M, Martinovic J, Whalen S, Taine L, Arveiler B, Lacombe D, Fergelot P. Van-Gils J, et al. Among authors: taine l. Clin Genet. 2019 Mar;95(3):420-426. doi: 10.1111/cge.13493. Epub 2019 Jan 11. Clin Genet. 2019. PMID: 30633342
Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes.
Doco-Fenzy M, Leroy C, Schneider A, Petit F, Delrue MA, Andrieux J, Perrin-Sabourin L, Landais E, Aboura A, Puechberty J, Girard M, Tournaire M, Sanchez E, Rooryck C, Ameil A, Goossens M, Jonveaux P, Lefort G, Taine L, Cailley D, Gaillard D, Leheup B, Sarda P, Geneviève D. Doco-Fenzy M, et al. Among authors: taine l. Eur J Hum Genet. 2014 Apr;22(4):471-9. doi: 10.1038/ejhg.2013.189. Epub 2013 Oct 16. Eur J Hum Genet. 2014. PMID: 24129437 Free PMC article.
[ORL and speech aspects in DiGeorge syndrome].
Portmann D, Marraco M, Lacombe D, Taine L, Gadan C, Siberchicot F. Portmann D, et al. Among authors: taine l. Rev Laryngol Otol Rhinol (Bord). 1997;118(4):273-8. Rev Laryngol Otol Rhinol (Bord). 1997. PMID: 9637100 Review. French.
Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.
Reboul MP, Tandonnet O, Biteau N, Belet-de Putter C, Rebouissoux L, Moradkhani K, Vu PY, Saura R, Arveiler B, Lacombe D, Taine L, Iron A. Reboul MP, et al. Among authors: taine l. Clin Genet. 2006 Sep;70(3):207-13. doi: 10.1111/j.1399-0004.2006.00664.x. Clin Genet. 2006. PMID: 16922723
63 results