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Results: 5

Authors: Granel, B Ravix, V Pedeillier, K Serratrice, J Disdier, P Voelckel, MA Mattei, JF Weiller, PJ
Citation: B. Granel et al., A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: A preliminary report, CLIN RHEUMA, 19(4), 2000, pp. 262-264

Authors: Missirian, C Moncla, A Voelckel, MA Ravix, V Philip, N
Citation: C. Missirian et al., Fragile X syndrome and 22q11.2 microdeletion in the same sibship, AM J MED G, 95(4), 2000, pp. 358-360

Authors: Chauve, X Missirian, C Malzac, P Girardot, L Guys, JM Louis, C Philip, N Voelckel, MA
Citation: X. Chauve et al., Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French family, AM J MED G, 95(1), 2000, pp. 10-12

Authors: Moncla, A Malzac, P Voelckel, MA Auquier, P Girardot, L Mattei, MG Philip, N Mattei, JF Lalande, M Livet, MO
Citation: A. Moncla et al., Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelmansyndrome patients, EUR J HUM G, 7(2), 1999, pp. 131-139

Authors: Moncla, A Malzac, P Livet, MO Voelckel, MA Mancini, J Delaroziere, JC Philip, N Mattei, JF
Citation: A. Moncla et al., Angelman syndrome resulting from UBE3A mutations in 14 patients from eightfamilies: clinical manifestations and genetic counselling, J MED GENET, 36(7), 1999, pp. 554-560
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