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Written information to patients in clinical genetics: what's the impact?
Cassini C, Thauvin-Robinet C, Vinault S, Binquet C, Coron F, Masurel-Paulet A, Bonithon-Kopp C, Mercier S, Joly L, Huet F, Faivre L. Cassini C, et al. Among authors: faivre l. Eur J Med Genet. 2011 May-Jun;54(3):277-80. doi: 10.1016/j.ejmg.2011.03.006. Epub 2011 Mar 21. Eur J Med Genet. 2011. PMID: 21420514
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndrome.
Faivre L, Nivelon-Chevallier A, Kottler ML, Robinet C, Khau Van Kien P, Lorcerie B, Munnich A, Maroteaux P, Cormier-Daire V, LeMerrer M. Faivre L, et al. Am J Med Genet. 2001 Mar 1;99(2):132-6. doi: 10.1002/1096-8628(2000)9999:999<00::aid-ajmg1135>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11241472 Review.
Hypochondroplasia and stature within normal limits: another family with an Asn540Ser mutation in the fibroblast growth factor receptor 3 gene.
Thauvin-Robinet C, Faivre L, Lewin P, De Monléon JV, François C, Huet F, Couailler JF, Campos-Xavier AB, Bonaventure J, Le Merrer M. Thauvin-Robinet C, et al. Among authors: faivre l. Am J Med Genet A. 2003 May 15;119A(1):81-4. doi: 10.1002/ajmg.a.10238. Am J Med Genet A. 2003. PMID: 12707965 No abstract available.
Unique survival in chrondrodysplasia-hermaphrodism syndrome.
Thauvin-Robinet C, Mugneret F, Callier P, Chouchane M, Garron E, Manceau E, Laurent N, Durand C, Nivelon-Chevallier A, Sapin E, Huet F, Faivre L. Thauvin-Robinet C, et al. Among authors: faivre l. Am J Med Genet A. 2005 Jan 30;132A(3):335-7. doi: 10.1002/ajmg.a.30417. Am J Med Genet A. 2005. PMID: 15578577 No abstract available.
756 results