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New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.
Vuillaume ML, Naudion S, Banneau G, Diene G, Cartault A, Cailley D, Bouron J, Toutain J, Bourrouillou G, Vigouroux A, Bouneau L, Nacka F, Kieffer I, Arveiler B, Knoll-Gellida A, Babin PJ, Bieth E, Jouret B, Julia S, Sarda P, Geneviève D, Faivre L, Lacombe D, Barat P, Tauber M, Delrue MA, Rooryck C. Vuillaume ML, et al. Among authors: tauber m. Am J Med Genet A. 2014 Aug;164A(8):1965-75. doi: 10.1002/ajmg.a.36587. Epub 2014 Apr 29. Am J Med Genet A. 2014. PMID: 24782328
[Normal puberty].
Cartault A, Edouard T, Pienkowski C, Tauber M. Cartault A, et al. Among authors: tauber m. Rev Prat. 2008 Jun 30;58(12):1311-6. Rev Prat. 2008. PMID: 18714651 Review. French.
French database of children and adolescents with Prader-Willi syndrome.
Molinas C, Cazals L, Diene G, Glattard M, Arnaud C, Tauber M; French Reference Centre for PWS (FrRefC-PWS). Molinas C, et al. Among authors: tauber m. BMC Med Genet. 2008 Oct 2;9:89. doi: 10.1186/1471-2350-9-89. BMC Med Genet. 2008. PMID: 18831731 Free PMC article.
[Child obesity].
Tauber M, Jouret B, Diene G. Tauber M, et al. Rev Prat. 2009 Sep 20;59(7):1005-12. Rev Prat. 2009. PMID: 19839478 French. No abstract available.
Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: new cases of "polyvalvular heart disease syndrome" or new association?
Edouard T, Prost-Squarcioni C, Dulac Y, Vaysse F, Cavé H, Saugier-Veber P, Bourrouillou G, Verloes A, Tauber M, Bieth E. Edouard T, et al. Among authors: tauber m. Eur J Med Genet. 2010 Jan-Feb;53(1):29-34. doi: 10.1016/j.ejmg.2009.11.002. Epub 2009 Nov 20. Eur J Med Genet. 2010. PMID: 19932204
774 results