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Results: 5

Authors: Faivre, L Nivelon-Chevallier, A Kottler, ML Robinet, C Van Kien, PK Lorcerie, B Munnich, A Maroteaux, P Cormier-Daire, V LeMerrer, M
Citation: L. Faivre et al., Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome, AM J MED G, 99(2), 2001, pp. 132-136

Authors: Mignon-Ravix, C Mugneret, F Stavropoulou, C Depetris, D Van Kien, PK Mattei, MG
Citation: C. Mignon-ravix et al., Maternally inherited duplication of the possible imprinted 14q31 region, J MED GENET, 38(5), 2001, pp. 343-347

Authors: Robinet, C Douvier, S Van Kien, PK Favre, B Luquet, I Nadal, N Nivelon-Chevallier, A Mugneret, F
Citation: C. Robinet et al., Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegaly, PRENAT DIAG, 20(11), 2000, pp. 936-938

Authors: Faivre, L Van Kien, PK Madinier-Chappat, N Nivelon-Chevallier, A Beer, F LeMerrer, M
Citation: L. Faivre et al., Can Hutchinson-Gilford progeria syndrome be a neonatal condition?, AM J MED G, 87(5), 1999, pp. 450-452

Authors: Luquet, I Favre, B Nadal, N Madinier, N Van Kien, PK Huet, F Nivelon-Chevallier, A Mugneret, F
Citation: I. Luquet et al., Two cases of terminal deletion of chromosome 13: Clinical features, conventional and molecular cytogenetic analysis, ANN GENET, 42(1), 1999, pp. 33-39
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