Olga Messina‐Baas

Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene.

Olga Messina‐Baas, Luz María González-Huerta, Sergio A. Cuevas‐Covarrubias · PubMed · 2006 · 48 citations

A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity.

Luz María González-Huerta, Olga Messina‐Baas, Sergio A. Cuevas‐Covarrubias · PubMed · 2007 · 22 citations

Molecular Analysis of the <i>CYP1B1</i> Gene: Identification of Novel Truncating Mutations in Patients with Primary Congenital Glaucoma

Olga Messina‐Baas, Luz María González-Huerta, Carmen Chima-Galán et al. · Ophthalmic Research · 2006 · 19 citations

Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report

Jaime Toral‐López, Luz María González-Huerta, Olga Messina‐Baas et al. · World Journal of Clinical Cases · 2020 · 17 citations · Full text

Familial Blau syndrome without uveitis caused by a novel mutation in the nucleotide‐binding oligomerization domain‐containing protein 2 gene with good response to infliximab

Jaime Toral‐López, Luz María González-Huerta, Mónica Martín‐del Campo et al. · Pediatric Dermatology · 2018 · 11 citations