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An intermediate phenotype in IDH related enchondromatosis spectrum.
Yilmaz-Gulec E, Marzin P, Huber-Lequesne C, Cormier-Daire V. Yilmaz-Gulec E, et al. Among authors: huber lequesne c. Eur J Med Genet. 2023 Mar;66(3):104697. doi: 10.1016/j.ejmg.2023.104697. Epub 2023 Jan 14. Eur J Med Genet. 2023. PMID: 36649847
Genotypes and phenotypes of children with SHOX deficiency in France.
Rosilio M, Huber-Lequesne C, Sapin H, Carel JC, Blum WF, Cormier-Daire V. Rosilio M, et al. Among authors: huber lequesne c. J Clin Endocrinol Metab. 2012 Jul;97(7):E1257-65. doi: 10.1210/jc.2011-3460. Epub 2012 Apr 19. J Clin Endocrinol Metab. 2012. PMID: 22518848