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Page 1
Craniofacial anomalies and malformations in respiratory chain deficiency.
Cormier-Daire V, Rustin P, Rötig A, Chrétien D, Le Merrer M, Belli D, Le Goff A, Hubert P, Ricour C, Munnich A. Cormier-Daire V, et al. Among authors: hubert p. Am J Med Genet. 1996 Dec 30;66(4):457-63. doi: 10.1002/(SICI)1096-8628(19961230)66:4<457::AID-AJMG15>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8989468
CHARGE syndrome: report of 47 cases and review.
Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S. Tellier AL, et al. Among authors: hubert p. Am J Med Genet. 1998 Apr 13;76(5):402-9. doi: 10.1002/(sici)1096-8628(19980413)76:5<402::aid-ajmg7>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9556299 Review.
Intestinal transplantation in children: preliminary experience in Paris.
Goulet O, Jan D, Lacaille F, Colomb V, Michel JL, Damotte D, Jouvet P, Brousse N, Faure C, Cézard JP, Sarnacki S, Peuchmaur M, Hubert P, Ricour C, Révillon Y. Goulet O, et al. Among authors: hubert p. JPEN J Parenter Enteral Nutr. 1999 Sep-Oct;23(5 Suppl):S121-5. doi: 10.1177/014860719902300530. JPEN J Parenter Enteral Nutr. 1999. PMID: 10483912
[Isolated neonatal dysfunction of brainstem].
Abadie V, Chéron G, Lyonnet S, Hubert P, Morisseau-Durand MP, Jan D, Manac'h Y, Couly G. Abadie V, et al. Among authors: hubert p. Arch Pediatr. 1996 Feb;3(2):130-6. doi: 10.1016/0929-693x(96)85063-9. Arch Pediatr. 1996. PMID: 8785532 French.
[Chronic septic granulomatosis revealed by neonatal pulmonary aspergillosis].
Mouy R, Ropert JC, Donadieu J, Hubert P, de Blic J, Revillon Y, Brunelle F, Schollet Martin S, Descamps B, Debré M, et al. Mouy R, et al. Among authors: hubert p. Arch Pediatr. 1995 Sep;2(9):861-4. doi: 10.1016/0929-693x(96)81264-4. Arch Pediatr. 1995. PMID: 7581783 French.
671 results