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Results: 1-6 |
Results: 6

Authors: Lia-Baldini, AS Muller, F Taillandier, A Gibrat, JF Mouchard, M Robin, B Simon-Bouy, B Serre, JL Aylsworth, AS Bieth, E Delanote, S Freisinger, P Hu, JCC Krohn, HP Nunes, ME Mornet, E
Citation: As. Lia-baldini et al., A molecular approach to dominance in hypophosphatasia, HUM GENET, 109(1), 2001, pp. 99-108

Authors: Megarbane, A Waked, N Chouery, E Moglabey, YB Saliba, N Mornet, E Serre, JL Slim, R
Citation: A. Megarbane et al., Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers, AM J MED G, 98(3), 2001, pp. 244-249

Authors: Greco, L Babron, MC Corazza, GR Percopo, S Sica, R Clot, F Fulchignoni-Lataud, MC Zavattari, P Momigliano-Richiardi, P Casari, G Gasparini, P Tosi, R Mantovani, V De Virgiliis, S Iacono, G D'Alfonso, A Selinger-Leneman, H Lemainque, A Serre, JL Clerget-Darpoux, F
Citation: L. Greco et al., Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families, ANN HUM GEN, 65, 2001, pp. 35-41

Authors: Clot, F Babron, MC Percopo, S Giordano, M Bouguerra, F Clerget-Darpoux, F Greco, L Serre, JL Fulchignoni-Lataud, MC
Citation: F. Clot et al., Study of two ectopeptidases in the susceptibility to celiac disease: Two newly identified polymorphisms of dipeptidylpeptidase IV, J PED GASTR, 30(4), 2000, pp. 464-466

Authors: Zurutuza, L Muller, F Gibrat, JF Taillandier, A Simon-Buoy, B Serre, JL Mornet, E
Citation: L. Zurutuza et al., Correlations of genotype and phenotype in hypophosphatasia, HUM MOL GEN, 8(6), 1999, pp. 1039-1046

Authors: Clot, F Fulchignoni-Lataud, MC Renoux, C Percopo, S Bouguerra, F Babron, MC Djilai-Saiah, I Caillat-Zucman, S Clerget-Darpoux, F Greco, L Serre, JL
Citation: F. Clot et al., Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations, TISSUE ANTI, 54(5), 1999, pp. 527-530
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