Nájera C - Search Results

1

[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. 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.

2

[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.

3

[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.

4

[Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].

Espinós C, Pérez-Garrigues H, Beneyto M, Vilela C, Rodrigo O, Nájera C. Espinós C, et al. Among authors: najera c. An Otorrinolaringol Ibero Am. 1999;26(1):83-95. An Otorrinolaringol Ibero Am. 1999. PMID: 10091368 Review. Spanish.

5

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

6

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

7

[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.

8

Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome.

Espinós C, Millán JM, Sánchez F, Beneyto M, Nájera C. Espinós C, et al. Among authors: najera c. Hum Genet. 1998 Jun;102(6):691-4. doi: 10.1007/s004390050763. Hum Genet. 1998. PMID: 9703432

9

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.

10

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

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

Search Page

Search Results