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:
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