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[Genetic counselling in visual and auditory disorders].
Millán JM, Aller E, Jaijo T, Grau E, Beneyto M, Nájera C. Millán JM, et al. Among authors: najera c. Arch Soc Esp Oftalmol. 2008 Dec;83(12):689-702. doi: 10.4321/s0365-66912008001200003. Arch Soc Esp Oftalmol. 2008. PMID: 19085640 Review. Spanish.
[Molecular genetics of pigmentary retinopathy].
Millán JM, Nájera C, Beneyto M. Millán JM, et al. Among authors: najera c. Med Clin (Barc). 1994 Jan 15;102(1):30-2. Med Clin (Barc). 1994. PMID: 8133683 Review. Spanish. No abstract available.
Identification of three novel mutations in the MYO7A gene.
Cuevas JM, Espinós C, Millán JM, Sánchez F, Trujillo MJ, Ayuso C, Beneyto M, Nájera C. Cuevas JM, et al. Among authors: najera c. Hum Mutat. 1999 Aug 19;14(2):181. doi: 10.1002/(SICI)1098-1004(1999)14:2<181::AID-HUMU11>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10447383
Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.
Jaijo T, Aller E, Oltra S, Beneyto M, Nájera C, Ayuso C, Baiget M, Carballo M, Antiñolo G, Valverde D, Moreno F, Vilela C, Perez-Garrigues H, Navea A, Millán JM. Jaijo T, et al. Among authors: najera c. Hum Mutat. 2006 Mar;27(3):290-1. doi: 10.1002/humu.9404. Hum Mutat. 2006. PMID: 16470552
[About genes and disease].
Nájera C, Beneyto M. Nájera C, et al. Med Clin (Barc). 1998 Apr 18;110(13):495-7. Med Clin (Barc). 1998. PMID: 9611731 Spanish. No abstract available.
Linkage analysis in Usher syndrome type I (USH1) families from Spain.
Espinós C, Nájera C, Millán JM, Ayuso C, Baiget M, Pérez-Garrigues H, Rodrigo O, Vilela C, Beneyto M. Espinós C, et al. Among authors: najera c. J Med Genet. 1998 May;35(5):391-8. doi: 10.1136/jmg.35.5.391. J Med Genet. 1998. PMID: 9610802 Free PMC article.
Genetics of retinoblastoma: a study.
Mateu E, Sánchez F, Nájera C, Beneyto M, Castell V, Hernández M, Serra I, Prieto F. Mateu E, et al. Among authors: najera c. Cancer Genet Cytogenet. 1997 May;95(1):40-50. doi: 10.1016/s0165-4608(96)00387-1. Cancer Genet Cytogenet. 1997. PMID: 9140452
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