Publications by authors named "Ines Pereiro"

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[Algorithm for the molecular analysis of Bardet-Biedl syndrome in Spain].
Sheila Castro-Sánchez, María Álvarez-Satta, Inés Pereiro, M Teresa Piñeiro-Gallego, Diana Valverde

Med Clin (Barc)· August 2015

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Clinical evaluation of two consanguineous families with homozygous mutations in BEST1.
Teresa Piñeiro-Gallego, María Álvarez, Inés Pereiro, Severiano Campos, Dror Sharon

Mol Vis· November 2011

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Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alström syndrome.
Ines Pereiro, Bethan E Hoskins, Jan D Marshall, Gayle B Collin, Jürgen K Naggert

Eur J Hum Genet· April 2011

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Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71.
Darryl Y Nishimura, Lisa M Baye, Rahat Perveen, Charles C Searby, Almudena Avila-Fernandez, Ines Pereiro

Am J Hum Genet· May 2010

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New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: detection of candidate regions by homozygosity mapping.
Ines Pereiro, Diana Valverde, Teresa Piñeiro-Gallego, Montserrat Baiget, Salud Borrego

Mol Vis· February 2010

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Complexity of phenotype-genotype correlations in Spanish patients with RDH12 mutations.
Diana Valverde, Ines Pereiro, Elena Vallespín, Carmen Ayuso, Salud Borrego

Invest Ophthalmol Vis Sci· March 2009

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