ACNP - Italian Periodicals Catalogue

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Results: 1-8 |

Results: 8

"Distraction" of grafted alveolar bone in cleft case using endosseous implant

Authors: Buis, J Rousseau, P Soupre, V Martinez, H Diner, PA Vazquez, MP

Citation: J. Buis et al., "Distraction" of grafted alveolar bone in cleft case using endosseous implant, CLEF PAL-CR, 38(4), 2001, pp. 405-409

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome

Authors: Gaston, V Le Bouc, Y Soupre, V Burglen, L Donadieu, J Oro, H Audry, G Vazquez, MP Gicquel, C

Citation: V. Gaston et al., Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome, EUR J HUM G, 9(6), 2001, pp. 409-418

Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P)

Authors: Houdayer, C Bonaiti-Pellie, C Erguy, C Soupre, V Dondon, MG Burglen, L Cougoureux, E Couderc, R Vazquez, MP Bahuau, M

Citation: C. Houdayer et al., Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P), AM J MED G, 104(1), 2001, pp. 86-92

Pierre Robin sequence and interstitial deletion 2q32.3-q33.2

Authors: Houdayer, C Portnoi, MF Vialard, F Soupre, V Crumiere, C Taillemite, JL Couderc, R Vazquez, JP Bahuau, M

Citation: C. Houdayer et al., Pierre Robin sequence and interstitial deletion 2q32.3-q33.2, AM J MED G, 102(3), 2001, pp. 219-226

Neurophysiological brainstem investigations in isolated Pierre Robin sequence

Authors: Renault, F Flores-Guevara, R Soupre, V Vazquez, MP Baudon, JJ

Citation: F. Renault et al., Neurophysiological brainstem investigations in isolated Pierre Robin sequence, EAR HUM DEV, 58(2), 2000, pp. 141-152

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome

Authors: Gaston, V Le Bouc, Y Soupre, V Vazquez, MP Gicquel, C

Citation: V. Gaston et al., Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome, HORMONE RES, 54(1), 2000, pp. 1-5

1q32-q41 microdeletion with reference to van der Woude syndrome and alliedclefting entities

Authors: Houdayer, C Soupre, V Karcenty, B Vazquez, MP Odent, S Lacombe, D Le Bouc, Y Munnich, A Bahuau, M

Citation: C. Houdayer et al., 1q32-q41 microdeletion with reference to van der Woude syndrome and alliedclefting entities, AM J MED G, 91(2), 2000, pp. 161-163

Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait

Authors: Houdayer, C Soupre, V Rosenberg-Bourgin, M Martinez, H Tredano, M Feldmann, D Feingold, J Aymard, P Munnich, A Le Bouc, Y Vazquez, MP Bahuau, M

Citation: C. Houdayer et al., Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait, ANN GENET, 42(2), 1999, pp. 69-74

Risultati: 1-8 |