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Results: 1-4 |
Results: 4

Authors: Fert-Ferrer, S Guichet, A Tantau, J Delezoide, AL Ozilou, C Romana, SP Gosset, P Viot, G Loison, S Moraine, C Morichon-Delvallez, N Turleau, C Vekemans, M Prieur, M
Citation: S. Fert-ferrer et al., Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features, PRENAT DIAG, 20(6), 2000, pp. 511-515

Authors: Sanlaville, D Aubry, MC Dumez, Y Nolen, MC Amiel, J Pinson, MP Lyonnet, S Munnich, A Vekemans, M Morichon-Delvallez, N
Citation: D. Sanlaville et al., Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up, J MED GENET, 37(7), 2000, pp. 525-528

Authors: Faivre, L Morichon-Delvallez, N Viot, G Larget-Piet, A Narcy, F Turleau, C Pinson, MP Dumez, Y Munnich, A Vekemans, M
Citation: L. Faivre et al., Prenatal diagnosis of a satellited non-acrocentric chromosome derived froma maternal translocation (10;13)(p13;p12) and review of literature, PRENAT DIAG, 19(3), 1999, pp. 282-286

Authors: Favire, L Morichon-Delvallez, N Viot, G Martinovic, J Pinson, MP Aubry, JP Raclin, V Edery, P Dumez, Y Munnich, A Vekemans, M
Citation: L. Favire et al., Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature, PRENAT DIAG, 19(1), 1999, pp. 49-53
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