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Results: 1-9 |
Results: 9

Authors: Tabet, AC Dupont, JM Lebbar, A Couturier-Turpin, MH Feldmann, G Rabineau, D
Citation: Ac. Tabet et al., Heteromorphism 18ph+: with or without reproductive consequences ?, ANN GENET, 44(3), 2001, pp. 139-142

Authors: Debuisschert, T Raffy, J Dupont, JM Pocholle, JP
Citation: T. Debuisschert et al., Nanosecond optical parametric oscillators, CR AC S IV, 1(5), 2000, pp. 561-583

Authors: Grange, G Thoury, A Dupont, JM Pannier, E LeRhun, F Souchet, MG Goffinet, F Cabrol, D
Citation: G. Grange et al., Sonographic measurement of the fetal iliac angle cannot be used alone as amarker for trisomy 21, FETAL DIAGN, 15(1), 2000, pp. 41-45

Authors: Kerjean, A Dupont, JM Vasseur, C Le Tessier, D Cuisset, L Paldi, A Jouannet, P Jeanpierre, M
Citation: A. Kerjean et al., Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis, HUM MOL GEN, 9(14), 2000, pp. 2183-2187

Authors: Le Tessier, D Dupont, JM Fichelson, S Bouscary, D Lebbar, A Dreyfus, F Rabineau, D
Citation: D. Le Tessier et al., Clonal chromosomal abnormalities identified by interphase fluorescence in situ hybridization on collagen cultured hematopoietic stem cells, LEUKEMIA, 14(5), 2000, pp. 949-950

Authors: Dupont, JM Deroussiaux, A Coquard, MP Lavorel, B Faucher, O Loete, M Jauslin, HR
Citation: Jm. Dupont et al., Dynamical stark effect in the nu(2)/nu(4) vibrational polyad of SiH4: Theory and observation, J MOL SPECT, 199(2), 2000, pp. 252-258

Authors: Grange, G Dupont, JM Jeanpierre, M
Citation: G. Grange et al., Genetics and intrauterine growth retardation, M S-MED SCI, 15(1), 1999, pp. 82-85

Authors: Bourc'his, D Miniou, P Jeanpierre, M Gomes, DM Dupont, JM De Saint-Basile, G Maraschio, P Tiepolo, L Viegas-Pequignot, E
Citation: D. Bourc'His et al., Abnormal methylation does not prevent X inactivation in ICF patients, CYTOG C GEN, 84(3-4), 1999, pp. 245-252

Authors: Dupont, JM Le Tessier, D Rabineau, D Cuisset, L Vasseur, C Jeanpierre, M Delpech, M Pinton, F Ponsot, G Denavit, MF
Citation: Jm. Dupont et al., Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome, J MED GENET, 36(8), 1999, pp. 652-654
Risultati: 1-9 |