Publicaciones ORCID
- 2026
- Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat Journal of Clinical Laboratory Analysis
- Trisomy 21 Variants Among 3,124 Mexican Patients with Down Syndrome: A Three-Decade Experience of a Referral Laboratory Archives of Medical Research
- 2025
- Fork Stalling and Template Switching in a Complex der(6)dn with Duplication of 6q24.3qter and 6p25.3: A Case Report Cytogenetic and Genome Research
- Severe Elimination Disorders and Normal Intelligence in a Case of MAP1B Related Syndrome: A Case Report Genes
- 2022
- A chromoanagenesis-driven ultra-complex t(5;7;21)dn truncates neurodevelopmental genes in a disabled boy as revealed by whole-genome sequencing European Journal of Medical Genetics
