T. Solans

Evaluation of RLBP1 in 50 autosomal recessive retinitis pigmentosa and 4 retinitis punctata albescens Spanish families

M. Baiget, C. Ayuso, D. Valverde, 2001, Ophthalmic genetics.

Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

M. Baiget, E. Tizzano, I. Hernán, 2008, Clinical genetics.

Clinical and genetic studies in Spanish patients with Usher syndrome type II: description of new mutations and evidence for a lack of genotype–phenotype correlation

M. Baiget, C. Ayuso, D. Valverde, 2005, Clinical genetics.

[Treatment of voice prosthesis leakage. Preliminary results].

A. Chays, M. Labrousse, J. Mérol, 2005, Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris.

Homozygous tandem duplication within the gene encoding the β‐subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa

M. Bayés, S. Amselem, M. Baiget, 1995 .

A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

M. Bayés, M. Baiget, D. Grinberg, 1998, Journal of medical genetics.

A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2 q 31-q 33 Monica Bayes

M. Baiget, D. Grinberg, S. Balcells, 2022 .

A novel mutation in exon 17 of the β-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family

M. Bayés, M. Baiget, D. Grinberg, 2004, Human Genetics.

A newautosomal recessive retinitis pigmentosa locus mapsonchromosome 2q31-q33

M. Baiget, D. Grinberg, A. Martinez-Mir, 2011 .