Rocio A. De La Cruz-Villafuerte
Monterrey, NLE, Mexico
Last Updated: 09/26/2026
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Found 9 publications
Should XYY syndrome be considered in the differential diagnosis of syndromic myopia? Apropos of a case.
Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: April 01, 2025
RPGR-Related Retinal Dystrophy in Latin America-A Collaborative Study.
Journal: American journal of ophthalmology
Published: March 12, 2025
A novel KMT2D gene variant c.6341del (p.Gly2114Alafs*30) and its phenotypic presentation in a Hispanic-Mexican woman with Kabuki syndrome: A case report.
Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: March 05, 2025
Spectrum of variants associated with inherited retinal dystrophies in Northeast Mexico.
Journal: BMC ophthalmology
Published: August 30, 2023
Multimodal and longitudinal evaluation of novel phenotype-genotype correlation of CLN3 isolated retinal degeneration in an hispanic female with heterozygous mutations c.944dup and c.1305C>G.
Journal: Ophthalmic genetics
Published: August 25, 2023
Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants.
Journal: Molecular genetics and genomics : MGG
Published: July 19, 2023
Case report: Disease phenotype associated with simultaneous biallelic mutations in ABCA4 and USH2A due to uniparental disomy of chromosome 1.
Journal: Frontiers in genetics
Published: May 20, 2022
Infrared meibography and molecular assessment of p63 gene mutations in a Mexican patient with EEC syndrome.
Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: March 23, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026