Publications by authors named "Veronica F Moran-Barroso"

8Publications

X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.

Authors:
Miguel A Noriega-Juárez Constanza García-Delgado América Villaseñor-Domínguez Carlos A Mena-Cedillos Mirna Toledo-Bahena Adriana Valencia-Herrera Patricia Baeza-Capetillo Alicia Cervantes Verónica F Morán-Barroso Nancy Monroy-Jaramillo

Bol Med Hosp Infant Mex 2020 ;77(4):212-217

Departamento de Genética, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Ciudad de México. México.

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January 2020

Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City.

Authors:
Silvia Martínez-Valverde Guillermo Salinas-Escudero Constanza García-Delgado Juan Garduño-Espinosa Verónica F Morán-Barroso Víctor Granados-García Ma Teresa Tiro-Sánchez Filiberto Toledano-Toledano Ma Vanessa Aldaz-Rodríguez

PLoS One 2019 10;14(1):e0208076. Epub 2019 Jan 10.

Programa de doctorado en Administración y Sistemas de Salud de la Universidad Nacional Autónoma de México, Mexico City, Mexico.

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September 2019

Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

Authors:
Nayla Y León-Carlos Constanza García-Delgado Ariadna B Morales-Jiménez Carlos Serrano-Bello Alicia Cervantes Verónica F Morán Barroso

Arch Argent Pediatr 2018 08;116(4):e603-e608

Departamento de Genética, Hospital Infantil de México Federico Gómez, Ciudad de México, México.

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August 2018

[Pallister-Killian syndrome in a Mexican mestizo patient. Case report].

Authors:
Paola Mendelsberg-Fishbein Constanza García-Delgado Linda B Muñoz-Martínez Maura Robledo-Cayetano Leonardo J Mejía-Marín Luis E Martínez-Barrera Mabel Cerrillo-Hinojosa Verónica F Moran-Barroso

Arch Argent Pediatr 2018 Feb;116(1):e135-e138

Departamento de Genética, Hospital Infantil de México Federico Gómez.

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February 2018

Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature.

Authors:
Rodrigo Pastrana-Ayala Gretty L Peña-Castro Adriana M Valencia-Herrera Carlos A Mena-Cedillos Sonia Toussaint-Caire Yumiko I Akaki-Carreño Constanza García-Delgado Veronica F Morán-Barroso Mirna Toledo-Bahena

Int J Dermatol 2017 Apr 19;56(4):435-439. Epub 2017 Feb 19.

Department of Dermatology, Hospital Infantil de México Federico Gómez, México, D.F, Mexico.

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April 2017

Caudal duplication with multicystic dysplastic kidney: a case report.

Authors:
Constanza García-Delgado Paola Mendelsberg-Fishbein Fernando González-Ledón Rodrigo Moreno-Salgado María E Blanco-Aguirre Verónica F Morán-Barroso

Clin Dysmorphol 2015 Jan;24(1):26-8

Departments of aGenetics bUrology, Hospital Infantil de México Federico Gómez, Mexico City cDepartment of Genetics, Hospital Materno Perinatal 'Mónica Pretelini Saenz', ISEM, Toluca, Mexico.

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January 2015

Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.

Authors:
Alicia Cervantes Constanza García-Delgado Fernando Fernández-Ramírez Carolina Galaz-Montoya Ariadna Berenice Morales-Jiménez Karem Nieto-Martínez Laura Gómez-Laguna Judith Villa-Morales Mónica Quintana-Palma Jaime Berúmen Susana Kofman Verónica F Morán-Barroso

BMC Med Genomics 2014 Sep 15;7:55. Epub 2014 Sep 15.

Departamento de Genética, Hospital Infantil de México Federico Gómez, Calle Dr, Márquez 162, Col, Doctores, Del, Cuauhtémoc, 06720 México, D,F,, México.

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September 2014

Genetic structure of three Native Mexican communities based on mtDNA haplogroups, and ABO and Rh blood group systems.

Authors:
Adriana Sánchez-Boiso Rosenda I Peñaloza-Espinosa Eduardo Castro-Sierra Ricardo M Cerda-Flores Leonora Buentello-Malo Rocío Sánchez-Urbina Rosa I Ortiz-de-luna Benjamín A Rodríguez-Espino Fabio A Salamanca-Gómez Martha P Flores-Ayón Teresita Salamanca-Vargas Jesús Aguirre-Hernández Elsa Cerón-Vázquez Juanita López-Castillejos Verónica F Morán-Barroso

Rev Invest Clin 2011 Nov-Dec;63(6):614-20

Departamento de Genética, Hospital Infantil de México Federico Gómez.

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June 2013