M. García-Hoyos

C. Ayuso, M. García-Hoyos, M. Trujillo-Tiebas, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Genotyping microarray: Mutation screening in Spanish families with autosomal dominant retinitis pigmentosa

M. Cortón, C. Ayuso, A. Avila-Fernandez, 2012, Molecular vision.

Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice.

J. Bennett, David S. Williams, S. Kim, 2008, The Journal of clinical investigation.

New approach for the refinement of the location of the X‐chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocation

C. Ayuso, M. García-Hoyos, D. Cantalapiedra, 2005, American journal of medical genetics. Part A.

A Comprehensive Analysis of Choroideremia: From Genetic Characterization to Clinical Practice

C. Rivolta, M. Cortón, C. Ayuso, 2016, PloS one.

Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

J. Rosell, M. Baiget, C. Ayuso, 2003, Journal of medical genetics.

Microdeletion found by array-CGH in girl with Blepharophimosis syndrome and apparently balanced translocation t(3;15)(q23;q25)

M. García-Hoyos, C. González-González, I. Lorda Sánchez, 2012, Ophthalmic genetics.

Detection of a Paternally Inherited Fetal Mutation in Maternal Plasma by the Use of Automated Sequencing

C. Ayuso, M. García-Hoyos, M. Trujillo-Tiebas, 2006, Annals of the New York Academy of Sciences.

Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.

C. Ayuso, M. García-Hoyos, D. Cantalapiedra, 2005, Molecular vision.

Novel UGT1A1 Gene Mutations in a Boy with Crigler–Najjar Syndrome Type II

M. García-Hoyos, A. Rodríguez-Dehli, D. Pérez-Solís, 2020, Journal of Pediatric Genetics.

Mutational screening of the RP2 and RPGR genes in Spanish families with X-linked retinitis pigmentosa.

J. Millán, C. Ayuso, M. García-Hoyos, 2006, Investigative ophthalmology & visual science.

Mutational Screening of the RP 2 and RPGR Genes in Spanish Families with X-Linked Retinitis Pigmentosa

J. Millán, C. Ayuso, M. García-Hoyos, 2006 .

Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

J. Rosell, M. Baiget, M. García-Hoyos, 2003, Journal of medical genetics.

Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism

P. Gómez-Garre, C. Ayuso, M. García-Hoyos, 2003, American journal of medical genetics. Part A.

Novel human pathological mutations. Gene symbol: LCA5. Disease: Leber Congenital Amaurosis (LCA).

E. Vallespín, C. Ayuso, A. Avila-Fernandez, 2010, Human genetics.

Novel Adeno-Associated Virus Serotypes Efﬁciently Transduce Murine Photoreceptors (cid:1)

C. Mussolino, James M. Wilson, E. Surace, 2007 .

Clinical description, molecular delineation and genotype–phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients

Lago, I. Mahillo, B. Gener, 2022, Journal of Medical Genetics.