VISIONS: the art of science. by Gil-Sanz, C, Martinez-Garay, I

The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody. by Martinez-Garay, I, Rustom, A, Gerdes, H, Kutsche, K

[Subtelomeric deletion 9qter: definition of the syndrome and parental origin in 2 patients]. by Roselló, M, Monfort, S, Orellana, C, Oltra, S, Martínez Garay, I, Martínez, F

A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region. by Martinez-Garay, I, Jablonka, S, Sutajova, M, Steuernagel, P, Gal, A, Kutsche, K

Reelin regulates cadherin function via Dab1/Rap1 to control neuronal migration and lamination in the neocortex. by Franco, S, Martinez-Garay, I, Gil-Sanz, C, Harkins-Perry, SR, Müller, U

Cajal-Retzius cells instruct neuronal migration by coincidence signaling between secreted and contact-dependent guidance cues. by Gil-Sanz, C, Franco, S, Martinez-Garay, I, Espinosa, A, Harkins-Perry, S, Müller, U

Cadherin2/4-signaling via PTP1B and catenins is critical for nucleokinesis during radial neuronal migration in the neocortex by Martinez-Garay, I, Gil-Sanz, C, Franco, S, Espinosa, A, Molnár, Z, Mueller, U

Dbx1-derived pyramidal neurons are generated locally in the developing murine neocortex by Rueda-Alana, E, Martinez-Garay, I, Encinas, J, Molnar, Z, Garcia-Moreno, F

Gypsy endogenous retrovirus maintains potential infectivity in several species of Drosophilids by Llorens, J, Clark, J, Martínez-Garay, I, Soriano, S, De Frutos, R, Martínez-Sebastián, M

Screening for Microdeletions of the X-Chromosome in Non-Specific Mental Retardation [2] by Martínez, F, Oltra, S, Berges, M, Orellana, C, Prieto, F, Martínez-Garay, I, Moltó, MD

The neuronal migration hypothesis of dyslexia: a critical evaluation 30 years on by Guidi, L, Velayos-Baeza, A, Martinez-Garay, I, Monaco, A, Paracchini, S, Bishop, D, Molnár, Z

Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family. by Martínez, F, Martínez-Garay, I, Oltra, S, Moltó, MD, Orellana, C, Monfort, S, Prieto, F, Tejada, I

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on by Guidi, LG, Velayos-Baeza, A, Martinez-Garay, I, Monaco, AP, Paracchini, S, Bishop, D, Molnar, Z

Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing by Guidi, L, Mattley, J, Martinez-Garay, I, Monaco, A, Linden, J, Velayos Baeza, A, Molnar, Z

Fate-restricted neural progenitors in the mammalian cerebral cortex. by Franco, S, Gil-Sanz, C, Martinez-Garay, I, Espinosa, A, Harkins-Perry, SR, Ramos, C, Müller, U

Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2. by Martínez, F, Martínez-Garay, I, Millán, J, Pérez-Aytes, A, Moltó, MD, Orellana, C, Prieto, F

Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome. by Martínez-Garay, I, Ballesta, M, Oltra, S, Orellana, C, Palomeque, A, Moltó, MD, Prieto, F, Martínez, F

Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum. by Orellana, C, Bernabeu, J, Monfort, S, Roselló, M, Oltra, S, Ferrer, I, Quiroga, R, Martínez-Garay, I, Martínez, F

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. by Martínez-Garay, I, Tomás, M, Oltra, S, Ramser, J, Moltó, MD, Prieto, F, Meindl, A, Kutsche, K, Martínez, F

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice. by Martinez-Garay, I, Guidi, L, Holloway, Z, Bailey, M, Lyngholm, D, Schneider, T, Donnison, T, Butt, S, Velayos-Baeza, A, Molnár, Z, Monaco, A