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Results: 1-11 |
Results: 11

Authors: De Baere, E Dixon, MJ Small, KW Jabs, EW Leroy, BP Devriendt, K Gillerot, Y Mortier, G Meire, F Van Maldergem, L Courtens, W Hjalgrim, H Huang, S Liebaers, I Van Regemorter, N Touraine, P Praphanphoj, V Verloes, A Udar, N Yellore, V Chalukya, M Yelchits, S De Paepe, A Kuttenn, F Fellous, M Veitia, R Messiaen, L
Citation: E. De Baere et al., Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation, HUM MOL GEN, 10(15), 2001, pp. 1591-1600

Authors: Ottolenghi, C Daizadeh, I Ju, A Kossida, S Renault, G Jacquet, M Fellous, A Gilbert, W Veitia, R
Citation: C. Ottolenghi et al., The genomic structure of C140rf1 is conserved across eukarya, MAMM GENOME, 11(9), 2000, pp. 786-788

Authors: Ottolenghi, C Veitia, R Quintana-Murci, L Torchard, D Scapoli, L Souleyreau-Therville, N Beckmann, J Fellous, M McElreavey, K
Citation: C. Ottolenghi et al., The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain, GENOMICS, 64(2), 2000, pp. 170-178

Authors: Ottolenghi, C Veitia, R Barbieri, M Fellous, M McElreavey, K
Citation: C. Ottolenghi et al., The human doublesex-related gene, DMRT2 is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript, GENOMICS, 64(2), 2000, pp. 179-186

Authors: Denamur, E Bocquet, N Baudouin, V Da Silva, F Veitia, R Peuchmaur, M Elion, J Gubler, MC Fellous, M Niaudet, P Loirat, C
Citation: E. Denamur et al., WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis, KIDNEY INT, 57(5), 2000, pp. 1868-1872

Authors: Veitia, R Ottolenghi, C
Citation: R. Veitia et C. Ottolenghi, Placing parallel stranded DNA in an evolutionary context, J THEOR BIO, 206(2), 2000, pp. 317-322

Authors: Saifi, GM Veitia, R El Khil, HK Barbaux, S Tilak, P Thomas, IM Fellous, M
Citation: Gm. Saifi et al., sY116, a human Y-linked polymorphic STS, J GENETICS, 79(1), 2000, pp. 17-20

Authors: Veitia, R David, S Barbier, P Vantard, M Gounon, P Bissery, MC Fellous, A
Citation: R. Veitia et al., Proteolysis of microtubule associated protein 2 and sensitivity of pancreatic tumours to docetaxel, BR J CANC, 83(4), 2000, pp. 544-549

Authors: Quintana-Murci, L Veitia, R Santachiara-Benerecetti, S McElreavey, K Fellous, M Bourgeron, T
Citation: L. Quintana-murci et al., Mitochondrial DNA, Y chromosome and human population history, M S-MED SCI, 15(8-9), 1999, pp. 974-982

Authors: Saifi, GM Tilak, P Veitia, R Thomas, IM Tharapel, A McElreavey, K Fellous, M Chandra, HS
Citation: Gm. Saifi et al., A novel mutation 5 ' to the HMG box of the SRY gene in a case of Swyer syndrome, J GENETICS, 78(3), 1999, pp. 157-161

Authors: Hurles, ME Veitia, R Arroyo, E Armenteros, M Bertranpetit, J Perez-Lezaun, A Bosch, E Shlumukova, M Cambon-Thomsen, A McElreavey, K de Munain, AL Rohl, A Wilson, IJ Singh, LJ Pandya, A Santos, FR Tyler-Smith, C Jobling, MA
Citation: Me. Hurles et al., Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism, AM J HU GEN, 65(5), 1999, pp. 1437-1448
Risultati: 1-11 |