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Results: 1-5 |
Results: 5

Authors: Olesen, C Hansen, C Bendsen, E Byskov, AG Schwinger, E Lopez-Pajares, I Jensen, PKA Kristoffersson, U Schubert, R Van Assche, E Wahlstroem, J Lespinasse, J Tommerup, N
Citation: C. Olesen et al., Identification of human candidate genes for male infertility by digital differential display, MOL HUM REP, 7(1), 2001, pp. 11-20

Authors: Lorda-Sanchez, I Lopez-Pajares, I Roche, MC Sanz, R de Alba, MR Gonzalez-Gonzalez, MC Ibanez, A Ramos, C Ayuso, C
Citation: I. Lorda-sanchez et al., Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child, AM J MED G, 95(4), 2000, pp. 336-338

Authors: Valero, R Marfany, G Gil-Benso, R Ibanez, MD Lopez-Pajares, I Prieto, F Rul-lan, G Sarret, E Gonzalez-Duarte, R
Citation: R. Valero et al., Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR, J MED GENET, 36(9), 1999, pp. 694-699

Authors: Wirth, J Nothwang, HG van der Maarel, S Menzel, C Borck, G Lopez-Pajares, I Brondum-Nielsen, K Tommerup, N Bugge, M Ropers, HH Haaf, T
Citation: J. Wirth et al., Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes, J MED GENET, 36(4), 1999, pp. 271-278

Authors: Satre, V Monnier, N Berthoin, F Ayuso, C Joannard, A Jouk, PS Lopez-Pajares, I Megabarne, A Philippe, HJ Plauchu, H Torres, ML Lunardi, J
Citation: V. Satre et al., Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene, AM J HU GEN, 65(1), 1999, pp. 68-76
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