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Results: 1-9 |
Results: 9
Connections of the auditory cortex with the claustrum and the endopiriformnucleus in the cat
Authors: Beneyto, M Prieto, JJ
Citation: M. Beneyto et Jj. Prieto, Connections of the auditory cortex with the claustrum and the endopiriformnucleus in the cat, BRAIN RES B, 54(5), 2001, pp. 485-498
Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations
Authors: Najera, C Sanchez, F Mateu, E Prieto, F Beneyto, M
Citation: C. Najera et al., Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations, MED CLIN, 116(10), 2001, pp. 365-372
A common ancestral origin of the frequent and widespread 2299delG USH2A mutation (vol 69, pg 228, 2001)
Authors: Dreyer, B Tranebjaerg, L Brox, V Rosenberg, T Moller, C Beneyto, M Weston, MD Kimberling, WJ Cremers, CWRJ Liu, XZ Nilssen, O
Citation: B. Dreyer et al., A common ancestral origin of the frequent and widespread 2299delG USH2A mutation (vol 69, pg 228, 2001), AM J HU GEN, 69(4), 2001, pp. 922-922
A common ancestral origin of the frequent and widespread 2299delG USH2A mutation
Authors: Dreyer, B Tranebjaerg, L Brox, V Rosenberg, T Moller, C Beneyto, M Weston, MD Kimberling, WJ Nilssen, O
Citation: B. Dreyer et al., A common ancestral origin of the frequent and widespread 2299delG USH2A mutation, AM J HU GEN, 69(1), 2001, pp. 228-234
A constitutional homozygous mutation in the RB1 gene in a patient with unilateral retinoblastoma
Authors: Sanchez, F Mateu, E Beneyto, M Najera, C Prieto, F
Citation: F. Sanchez et al., A constitutional homozygous mutation in the RB1 gene in a patient with unilateral retinoblastoma, J MED GENET, 37(8), 2000, pp. 615-620
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa
Authors: Miano, MG Testa, F Strazzullo, M Trujillo, M De Bernardo, C Grammatico, B Simonelli, F Mangino, M Torrente, I Ruberto, G Beneyto, M Antinolo, G Rinaldi, E Danesino, C Ventruto, V D'Urso, M Ayuso, C Baiget, M Ciccodicola, A
Citation: Mg. Miano et al., Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa, EUR J HUM G, 7(6), 1999, pp. 687-694
Specific staining of nonpyramidal cell populations of the cerebral cortex by lectin cytochemistry on semithin sections
Authors: Beneyto, M Rueda, J Merchan, JA Prieto, JJ
Citation: M. Beneyto et al., Specific staining of nonpyramidal cell populations of the cerebral cortex by lectin cytochemistry on semithin sections, BRAIN RES B, 49(4), 1999, pp. 251-262
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain
Authors: Millan, JM Martinez, F Cadroy, A Gandia, J Casquero, M Beneyto, M Badin, L Prieto, F
Citation: Jm. Millan et al., Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain, CLIN GENET, 56(1), 1999, pp. 98-99
Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib
Authors: Cuevas, JM Espinos, C Millan, JM Sanchez, F Trujillo, MJ Garcia-Sandoval, B Ayuso, C Najera, C Beneyto, M
Citation: Jm. Cuevas et al., Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib, MOL CELL PR, 12(6), 1998, pp. 417-420
Risultati: 1-9 |