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Concha Vilela

10

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Electroretinogram Alterations in Diabetes

2011
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Citations (2)
Mutation Profile of the MYO7A Gene in Spanish Patients With Usher Syndrome Type I

2006 Human Mutation
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Citations (42)
Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II

2006 Journal of Medical Genetics
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[Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].

1999 Anales otorrinolaringológicos ibero-americanos
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Citations (1)
Linkage analysis in Usher syndrome type I (USH1) families from Spain.

1998 Journal of Medical Genetics
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Citations (18)
Putative association of a mutant ROM1 allele with retinitis pigmentosa.

1997 Human Genetics
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Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP)

1996 Ophthalmic Genetics
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Citations (1)
An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q

1995 Human Genetics
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Citations (13)