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Results: 1-6 |
Results: 6

Authors: Vital, A Ferrer, X Lagueny, A Vandenberghe, A Latour, P Goizet, C Canron, MH Louiset, P Petry, KG Vital, C
Citation: A. Vital et al., Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations, J PERIPH N, 6(2), 2001, pp. 79-84

Authors: Coupry, I Taine, L Goizet, C Soriano, C Mortemousque, B Arveiler, B Lacombe, D
Citation: I. Coupry et al., Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion, J MED GENET, 38(1), 2001, pp. 35-38

Authors: Rodriguez, D Gauthier, F Bertini, E Bugiani, M Brenner, M N'guyen, S Goizet, C Gelot, A Surtees, R Pedespan, JM Hernandorena, X Troncoso, M Uziel, G Messing, A Ponsot, G Pham-Dinh, D Dautigny, A Boespflug-Tanguy, O
Citation: D. Rodriguez et al., Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation, AM J HU GEN, 69(5), 2001, pp. 1134-1140

Authors: Goizet, C Excoffier, E Taine, L Taupiac, E El Moneim, AA Arveiler, B Bouvard, M Lacombe, D
Citation: C. Goizet et al., Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH, AM J MED G, 96(6), 2000, pp. 839-844

Authors: Battin, J Lacombe, D Taine, L Goizet, C
Citation: J. Battin et al., Williams syndrome and behavioral phenotypes in human microdeletion syndromes, B ACA N MED, 184(1), 2000, pp. 105-116

Authors: Goizet, C Bonneau, D Lacombe, D
Citation: C. Goizet et al., W syndrome: Report of three cases and review, AM J MED G, 87(5), 1999, pp. 446-449
Risultati: 1-6 |