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Results: 1-4 |
Results: 4

Authors: Saugier-Veber, P Drouot, N Wolf, LM Kuhn, JM Frebourg, T Lefebvre, H
Citation: P. Saugier-veber et al., Identification of a novel mutation in the autoimmune regulator (AIRE-1) gene in a French family with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, EUR J ENDOC, 144(4), 2001, pp. 347-351

Authors: Saugier-Veber, P Drouot, N Lefebvre, S Charbonnier, F Vial, E Munnich, A Frebourg, T
Citation: P. Saugier-veber et al., Detection of heterozygous SMN1 deletions in SMA families using a simple fluorescent multiplex PCR method, J MED GENET, 38(4), 2001, pp. 240-243

Authors: Charbonnier, F Raux, G Wang, Q Drouot, N Cordier, F Limacber, JM Saurin, JC Puisieux, A Olschwang, S Frebourg, T
Citation: F. Charbonnier et al., Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments, CANCER RES, 60(11), 2000, pp. 2760-2763

Authors: Paternotte, C Rudnicki, D Fizames, C Davoine, CS Mavel, D Durr, A Samson, D Marquette, C Muselet, D Vega-Czarny, N Drouot, N Voit, T Fontaine, B Gyapay, G Auburger, G Weissenbach, J Hazan, J
Citation: C. Paternotte et al., Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q, GENOME RES, 8(11), 1998, pp. 1216-1227
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