Mireya Vela-Orozco
Guadalajara, JAL, Mexico
Last Updated: 09/26/2026
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Found 10 publications
Clonal Profiles in a Li-Fraumeni Syndrome Patient With SHH Medulloblastoma: Clonal Evolution, Genomics, and Clinical Implications.
Journal: Pediatric blood & cancer
Published: September 11, 2025
Spectrum of Germline Cytogenomic Alterations in RB1 in Mexican Patients With Retinoblastoma.
Journal: Pediatric blood & cancer
Published: September 10, 2025
Evaluation of NOS3 894G>T (p.Glu298Asp) Variant as Risk Factor for Open Neural Tube Defects in Infants from Western Mexico.
Journal: Genetic testing and molecular biomarkers
Published: August 29, 2025
ICAM1 778G>A (rs1799969), ADD1 1378G>T (rs4961), NPPA 553T>C (rs5065), and NOS3 894G>T (rs1799983) Variants in Infants with Gastroschisis from Western Mexico.
Journal: Genetic testing and molecular biomarkers
Published: May 27, 2025
MTHFR 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico.
Journal: Genetic testing and molecular biomarkers
Published: May 08, 2024
TRAPPC11-CDG muscular dystrophy: Review of 54 cases including a novel patient.
Journal: Molecular genetics and metabolism
Published: January 24, 2024
Complete blood count differences in a cohort of Down syndrome neonates with transient abnormal myelopoiesis screened for GATA1 pathogenic variants.
Journal: American journal of medical genetics. Part A
Published: December 24, 2019
Prevalence and risk factors for Down syndrome: A hospital-based single-center study in Western Mexico.
Journal: American journal of medical genetics. Part A
Published: September 09, 2018
Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
Journal: Congenital anomalies
Published: June 02, 2018
Descriptive study of the complete blood count in newborn infants with Down syndrome.
Journal: American journal of medical genetics. Part A
Published: April 29, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026