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Results: 1-5 |
Results: 5

Authors: Essenfelder, GM Lamartine, J Waksman, G
Citation: Gm. Essenfelder et al., Connexins and hereditary human diseases, M S-MED SCI, 17(2), 2001, pp. 244-246

Authors: Lamartine, J Essenfelder, GM Kibar, Z Lanneluc, I Callouet, E Laoudj, D Lemaitre, G Hand, C Hayflick, SJ Zonana, J Antonarakis, S Radhakrishna, U Kelsell, DP Christianson, AL Pitaval, A Der Kaloustian, V Fraser, C Blanchet-Bardon, C Rouleau, GA Waksman, G
Citation: J. Lamartine et al., Mutations in GJB6 cause hidrotic ectodermal dysplasia, NAT GENET, 26(2), 2000, pp. 142-144

Authors: Lamartine, J Pitaval, A Soularue, P Lanneluc, I Lemaitre, G Kibar, Z Rouleau, GA Waksman, G
Citation: J. Lamartine et al., A 1.5-mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11, GENOMICS, 67(2), 2000, pp. 232-236

Authors: Lamartine, J Laoudj, D Blanchet-Bardon, C Kibar, Z Soularue, P Ridoux, V Dubertret, L Rouleau, GA Waksman, G
Citation: J. Lamartine et al., Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family, BR J DERM, 142(2), 2000, pp. 248-252

Authors: Mertens, G Gielis, M Mommers, N Mularoni, A Lamartine, J Heylen, H Muylle, L Vandenberghe, A
Citation: G. Mertens et al., Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles, INT J LEGAL, 112(3), 1999, pp. 192-194
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