Get started
Author

Verónica Fabiola Morán-Barroso

Observed names: V F Moran-Barroso, V F Morán-Barroso, V. F. Morán-Barroso, V.F. Morán-Barroso, V.F. Morán‐Barroso, Veronica F. Morán‐Barroso, Veronica Fabiola Morán-Barroso, Veronica Moran-Barroso, Verónica F Moran-Barroso, Verónica F Morán Barroso, Verónica F Morán-Barroso, Verónica F Morán-barroso, Verónica F. Morán-Barroso, Verónica Fabiola Morán Barroso, Verónica Fabiola Morán-Barr, Verónica Fabiola Morán‐Barroso, Verónica Morán Barroso, Verónica Morán‐Barroso, VerónicaF Morán-Barroso
ORCID: 0000-0001-8256-7729
Observed ORCIDs: 0000-0001-8256-7729, 0000-0002-3768-9687
OpenAlex ID: A5019861369
Cytogenetic Profile in 1,921 Cases of Trisomy 21 Syndrome
2015 · Francisco Flores-Ramírez, Claudia Palacios-Guerrero, et al. · Archives of Medical Research · 43
Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population
2013 · Edgar Ricardo Vázquez-Martínez, Gustavo Varela-Fascinetto, et al. · Meta Gene · 18
PDF
CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract.
2005 · Juan Carlos Zenteno, Maria Elena Morales, et al. · PubMed · 16
Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population
2019 · Magdalena Cerón-Rodríguez, Edgar Ricardo Vázquez-Martínez, et al. · Annals of Hepatology · 15
PDF
Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature
2017 · Laura Gómez-Laguna, Alejandro Martínez-Herrera, et al. · Ophthalmic Genetics · 15
Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event
2021 · Verónica Fabiola Morán‐Barroso, Alicia Cervantes, et al. · Molecular Genetics & Genomic Medicine · 12
PDF
Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease
2015 · Candy Sue Márquez-Ávila, Alfredo Vizcaíno-Alarcón, et al. · International Journal of Pediatric Otorhinolaryngology · 11
Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome
2013 · M. Abreu-González, C. García-Delgado, et al. · Case Reports in Genetics · 11
PDF
Congenital hearing loss: a literature review of the genetic etiology in a Mexican population
2022 · Carlos De la Torre-González, Dina Villanueva-García, et al. · Boletín Médico del Hospital Infantil de México · 10
PDF
Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City
2019 · Silvia Martínez-Valverde, Guillermo Salinas-Escudero, et al. · PLoS ONE · 10
PDF
Macroglosia congénita: características clínicas y estrategias de tratamiento en la edad pediátrica
2016 · Paulina María Núñez-Martínez, Constanza García-Delgado, et al. · Boletín Médico del Hospital Infantil de México · 10
PDF
Microtia-atresia: aspectos clínicos, genéticos y genómicos
2014 · Mónica Aguinaga-Ríos, Sara Frías, et al. · Boletín Médico del Hospital Infantil de México · 8
PDF
Contribution of next generation sequencing to the diagnosis of inborn errors of immunity in a pediatric cohort
2025 · Guadalupe Fernanda Godinez-Zamora, Patricia Baeza-Capetillo, et al. · Frontiers in Immunology · 6
PDF
Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia
2017 · N. Monroy‐Jaramillo, J.D. Abad‐Flores, et al. · Journal of the European Academy of Dermatology and Venereology · 6
Congenital macroglossia: clinical features and therapeutic strategies in pediatric patients
2016 · Paulina María Núñez-Martínez, Constanza García-Delgado, et al. · Boletín Médico Del Hospital Infantil de México (English Edition) · 6
PDF
Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012
2014 · Carolina Isabel Galaz-Montoya, Constanza García-Delgado, et al. · Boletín Médico del Hospital Infantil de México · 6
PDF
Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities ( CDAGS syndrome): first report in a Mexican patient and review of the literature
2017 · Rodrigo Pastrana‐Ayala, Gretty L. Peña‐Castro, et al. · International Journal of Dermatology · 5
Perfi l clínico de una cohorte de pacientes con síndrome de Beckwith-Wiedemann atendidos en el Hospital Infantil de México Federico Gómez de 2007 a 2012 Clinical profi le of a patient cohort with Beckwith-Wiedemann syndrome treated at the Hospital Infantil de México Federico Gómez (2007 to 2012)
2013 · Rodrigo Moreno‐Salgado, Constanza García‐Delgado, et al. · Boletín Médico del Hospital Infantil de México · 5
Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems.
2011 · Adriana Sánchez-Boiso, Rosenda I Peñaloza-Espinosa, et al. · PubMed · 5
A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.
2010 · C García-Delgado, E Bahena-Martínez, et al. · PubMed · 5
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
2014 · Alicia Cervantes, Constanza García-Delgado, et al. · BMC Medical Genomics · 4
PDF
Displasia ectodérmica hipohidrótica ligada al cromosoma X de novo por variante recurrente en un paciente mexicano
2020 · Miguel A. Noriega-Juárez, Constanza García-Delgado, et al. · Boletín Médico del Hospital Infantil de México · 3
PDF
A Novel c.91dupG JAG1 Gene Mutation Is Associated with Early Onset and Severe Alagille Syndrome
2018 · Alejandra del Pilar Reyes-de la Rosa, Gustavo Varela-Fascinetto, et al. · Case Reports in Genetics · 3
PDF
Congenital hypertrichosis universalis in Mexican female twins
2015 · Alicia Cervantes, Constanza García‐Delgado, et al. · International Journal of Dermatology · 3
Escobar syndrome with heterotaxia and esophageal atresia: case report.
2014 · L E Martínez-Barrera, V F Morán-Barroso, et al. · PubMed · 3
Works count: 47
Citation count: 259
H-index: 10
I10-index: 11
Year
Topic
Type