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11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.
Netchine I, Rossignol S, Dufourg MN, Azzi S, Rousseau A, Perin L, Houang M, Steunou V, Esteva B, Thibaud N, Demay MC, Danton F, Petriczko E, Bertrand AM, Heinrichs C, Carel JC, Loeuille GA, Pinto G, Jacquemont ML, Gicquel C, Cabrol S, Le Bouc Y. Netchine I, et al. Among authors: cabrol s. J Clin Endocrinol Metab. 2007 Aug;92(8):3148-54. doi: 10.1210/jc.2007-0354. Epub 2007 May 15. J Clin Endocrinol Metab. 2007. PMID: 17504900
Molecular diagnosis of Turner's syndrome.
Gicquel C, Cabrol S, Schneid H, Girard F, Le Bouc Y. Gicquel C, et al. Among authors: cabrol s. J Med Genet. 1992 Aug;29(8):547-51. doi: 10.1136/jmg.29.8.547. J Med Genet. 1992. PMID: 1355559 Free PMC article.
Cardiovascular findings and management in Turner syndrome: insights from a French cohort.
Donadille B, Rousseau A, Zenaty D, Cabrol S, Courtillot C, Samara-Boustani D, Salenave S, Monnier-Cholley L, Meuleman C, Jondeau G, Iserin L, Duranteau L, Cabanes L, Bourcigaux N, Bonnet D, Bouchard P, Chanson P, Polak M, Touraine P, Lebouc Y, Carel JC, Léger J, Christin-Maitre S. Donadille B, et al. Among authors: cabrol s. Eur J Endocrinol. 2012 Oct;167(4):517-22. doi: 10.1530/EJE-12-0434. Epub 2012 Jul 16. Eur J Endocrinol. 2012. PMID: 22802424 Free article.
Final height in Turner syndrome patients treated with growth hormone.
Rochiccioli P, Battin J, Bertrand AM, Bost M, Cabrol S, le Bouc Y, Chaussain JL, Chatelain P, Colle M, Czernichow P, et al. Rochiccioli P, et al. Among authors: cabrol s. Horm Res. 1995;44(4):172-6. doi: 10.1159/000184620. Horm Res. 1995. PMID: 8522279 Clinical Trial.
90 results