Izabel M. Flores-Rios
Guadalajara, JAL, Mexico
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
MTHFR C677T and A1298C Gene Variants in Patients with Turner Syndrome and Their Mothers.
Journal: Genetic testing and molecular biomarkers
Published: April 20, 2026
A Family with EEC Syndrome in the Son and ADULT Syndrome in His Father Caused by the c.797G>A (p.Arg266Gln) Pathogenic Variant in the TP63 Gene.
Journal: Molecular syndromology
Published: May 02, 2023
Usefulness of the MS-MLPA technique in the diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
Journal: Gaceta medica de Mexico
Published: October 18, 2022
Prader-Willi and Angelman syndromes: case series diagnosed by MS-MLPA assay
Journal: Revista medica del Instituto Mexicano del Seguro Social
Published: January 18, 2021
Acute liver failure in a male patient with NGLY1-congenital disorder of deglycosylation.
Journal: European journal of medical genetics
Published: January 13, 2020
Maternal risk factors for congenital heart defects in infants with Down syndrome from Western Mexico.
Journal: American journal of medical genetics. Part A
Published: January 19, 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
Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.
Journal: Congenital anomalies
Published: September 16, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026