| 1 | Duplication of 12q24.21q24.33 in a Girl with Epilepsy, Expanding the Phenotype | Coautor: Messina-Baas, Olga, Plaza-Benhumea, Lautaro, Martin-de Saro, Monica D., Sanchez-Acosta, Cesar G., et al. | 2022 | Molecular Syndromology | WoS-id: 000773291000001
Scopus-id: 2-s2.0-85126998314
| 0 | 0 |
| 2 | A novel case of a girl with partial trisomy 12q24.21q24.33 and review of the literature | Coautor: Messina-Baas, Olga, Plaza-Benhumea, Lautaro, Martin-DeSaro, Monica, Cuevas-Covarrubias, Sergio | 2022 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 000779367702165
| 0 | 0 |
| 3 | Expanding phenotype in a patient with partial trisomy 13q/monosomy 3p resulting from a paternal reciprocal 3p;13q translocation | Coautor: Messina-Baas, Olga, Martin-DeSaro, Monica, Plaza-Benhumea, Lautaro, Gonzalez-Huerta, Luz, et al. | 2022 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 000779367702166
| 0 | 0 |
| 4 | Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy | Coautor: Messina-Baas, Olga, Martin-de Saro, Monica, Compean, Zyndia, Aguilar, Karina, et al. | 2021 | Molecular Syndromology | WoS-id: 000675445100001
Scopus-id: 2-s2.0-85111565233
| 1 | 2 |
| 5 | 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 | Coautor: Messina-Baas, Olga, Toral-Lopez, Jaime, Huerta, Luz Maria Gonzalez, Cuevas-Covarrubias, Sergio A. | 2020 | World Journal Of Clinical Cases | WoS-id: 000595692200019
Scopus-id: 2-s2.0-85105883364
| 4 | 6 |
| 6 | Whole exome sequencing reveals NM_005267.4: c.130G > A mutation in GJA8 gene in a large Mexican family with autosomal dominant cataract | 1ᵉʳ autor: Messina-Baas, O., Gonzalez-Huerta, L., Vega-Gama, R., Cuevas-Covarrubias, S. | 2018 | EUROPEAN JOURNAL OF HUMAN GENETICS | WoS-id: 000489312607056
| 0 | 0 |
| 7 | A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the Phenotype | Coautor: Messina Baas, Olga, Toral-Lopez, Jaime, Gonzalez-Huerta, Luz M., Cuevas-Covarrubias, Sergio A. | 2016 | Molecular Syndromology | WoS-id: 000393169100006
Scopus-id: 2-s2.0-84961390924
| 2 | 4 |
| 8 | Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract | 1ᵉʳ autor: Messina-Baas, Olga, Gonzalez-Garay, Manuel L., Gonzalez-Huerta, Luz M., Toral-Lopez, Jaime, et al. | 2016 | Molecular Syndromology | WoS-id: 000393169400006
Scopus-id: 2-s2.0-84963499822
| 4 | 7 |
