Beneyto M - Search Results

1

[Usher syndrome: an example of genetic heterogeneity].

Nájera C, Beneyto M, Millán JM. Nájera C, et al. Among authors: beneyto m. Med Clin (Barc). 2005 Oct 1;125(11):423-7. doi: 10.1157/13079387. Med Clin (Barc). 2005. PMID: 16216190 Review. Spanish.

2

Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.

Nájera C, Beneyto M, Blanca J, Aller E, Fontcuberta A, Millán JM, Ayuso C. Nájera C, et al. Among authors: beneyto m. Hum Mutat. 2002 Jul;20(1):76-7. doi: 10.1002/humu.9042. Hum Mutat. 2002. PMID: 12112664

3

Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome.

Aller E, Jaijo T, Beneyto M, Nájera C, Morera C, Pérez-Garrigues H, Ayuso C, Millán J. Aller E, et al. Among authors: beneyto m. Ophthalmic Genet. 2007 Sep;28(3):151-5. doi: 10.1080/13816810701537374. Ophthalmic Genet. 2007. PMID: 17896313

4

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

Jaijo T, Aller E, García-García G, Aparisi MJ, Bernal S, Avila-Fernández A, Barragán I, Baiget M, Ayuso C, Antiñolo G, Díaz-Llopis M, Külm M, Beneyto M, Nájera C, Millán JM. Jaijo T, et al. Among authors: beneyto m. Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1311-7. doi: 10.1167/iovs.09-4085. Epub 2009 Aug 13. Invest Ophthalmol Vis Sci. 2010. PMID: 19683999

5

[Molecular genetics of pigmentary retinopathy].

Millán JM, Nájera C, Beneyto M. Millán JM, et al. Among authors: beneyto m. Med Clin (Barc). 1994 Jan 15;102(1):30-2. Med Clin (Barc). 1994. PMID: 8133683 Review. Spanish. No abstract available.

6

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: beneyto m. 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.

7

[Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations].

Nájera C, Sánchez F, Mateu E, Prieto F, Beneyto M. Nájera C, et al. Among authors: beneyto m. Med Clin (Barc). 2001 Mar 17;116(10):365-72. doi: 10.1016/s0025-7753(01)71832-5. Med Clin (Barc). 2001. PMID: 11333669 Spanish.

8

[Molecular genetic study of Usher syndrome in Spain].

Jaijo T, Aller E, Beneyto M, Nájera C, Millán JM. Jaijo T, et al. Among authors: beneyto m. Acta Otorrinolaringol Esp. 2005 Aug-Sep;56(7):285-9. doi: 10.1016/s0001-6519(05)78616-7. Acta Otorrinolaringol Esp. 2005. PMID: 16240916 Free article. Spanish.

9

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: beneyto m. Hum Mutat. 2006 Mar;27(3):290-1. doi: 10.1002/humu.9404. Hum Mutat. 2006. PMID: 16470552

10

Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II.

Aller E, Jaijo T, Beneyto M, Nájera C, Oltra S, Ayuso C, Baiget M, Carballo M, Antiñolo G, Valverde D, Moreno F, Vilela C, Collado D, Pérez-Garrigues H, Navea A, Millán JM. Aller E, et al. Among authors: beneyto m. J Med Genet. 2006 Nov;43(11):e55. doi: 10.1136/jmg.2006.041764. J Med Genet. 2006. PMID: 17085681 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

113 results

Search Page