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[Smith-Lemli-Opitz syndrome].
Pelluard-Nehmé F, Carles D, Alberti EM, Saura R, Wong C, Wolf C. Pelluard-Nehmé F, et al. Ann Pathol. 2005 Sep;25(4):318-21. doi: 10.1016/s0242-6498(05)80136-1. Ann Pathol. 2005. PMID: 16327658 French.
Multicentric infantile myofibromatosis: two perinatal cases.
Pelluard-Nehmé F, Coatleven F, Carles D, Alberti EM, Briex M, Dallay D. Pelluard-Nehmé F, et al. Eur J Pediatr. 2007 Oct;166(10):997-1001. doi: 10.1007/s00431-006-0369-8. Epub 2006 Dec 21. Eur J Pediatr. 2007. PMID: 17186271
Molecular heterogeneity in fetal forms of type II lissencephaly.
Bouchet C, Gonzales M, Vuillaumier-Barrot S, Devisme L, Lebizec C, Alanio E, Bazin A, Bessières-Grattagliano B, Bigi N, Blanchet P, Bonneau D, Bonnières M, Carles D, Delahaye S, Fallet-Bianco C, Figarella-Branger D, Gaillard D, Gasser B, Guimiot F, Joubert M, Laurent N, Liprandi A, Loget P, Marcorelles P, Martinovic J, Menez F, Patrier S, Pelluard-Nehmé F, Perez MJ, Rouleau-Dubois C, Triau S, Laquerrière A, Encha-Razavi F, Seta N. Bouchet C, et al. Among authors: pelluard nehme f. Hum Mutat. 2007 Oct;28(10):1020-7. doi: 10.1002/humu.20561. Hum Mutat. 2007. PMID: 17559086