| 1 | Silver-Russell syndrome caused by trisomy 11p15.5 due to a derivative X chromosome from a de novo t(X;11) in a Mexican female patient | Coautor: Morán-Barroso V.F., Paz-Ramírez M., Muñoz-Martínez L.B., Morales-Jiménez A.B., et al. | 2022 | CLINICAL DYSMORPHOLOGY | WoS-id: 000763577900009
Scopus-id: 2-s2.0-85125682553
| 0 | 0 |
| 2 | Congenital hearing loss: a literature review of the genetic etiology in a Mexican population | Coautor: Morán-Barroso V.F., de la Torre-González C., Villanueva-García D., García-Delgado C., et al. | 2022 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | WoS-id: 000861817400002
Scopus-id: 2-s2.0-85137773630
| 3 | 3 |
| 3 | 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 | 1ᵉʳ autor: Fabiola Moran-Barroso, Veronica, Cervantes, Alicia, del Refugio Rivera-Vega, Maria, del Castillo-Moreno, Adriana, et al. | 2021 | Molecular Genetics & Genomic Medicine | WoS-id: 000674868400001
Scopus-id: 2-s2.0-85110692137
| 2 | 2 |
| 4 | Displasia ectodérmica hipohidrótica ligada al cromosoma X de novo por variante recurrente en un paciente mexicano | Coautor: Morán-Barroso V.F., Noriega-Juárez M.A., García-Delgado C., Villaseñor-Domínguez A., et al. | 2020 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | WoS-id: 000551909000008
Scopus-id: 2-s2.0-85088622686
| 2 | 3 |
| 5 | High penetrance of EDA pathogenic variants in Mexican female carriers with hypohidrotic ectodermal dysplasia | Coautor: Morán-Barroso V., García-Delgado C., Noriega-Juárez M., Cervantes A., et al. | 2020 | DERMATOLOGICA SINICA | WoS-id: 000601214900006
Scopus-id: 2-s2.0-85091512458
| 0 | 0 |
| 6 | Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City | Coautor: Morán-Barroso V.F., Martínez-Valverde S., Salinas-Escudero G., García-Delgado C., et al. | 2019 | PLOS ONE | WoS-id: 000455483000010
Scopus-id: 2-s2.0-85059815340
| 4 | 5 |
| 7 | Microdeletion 22q11.2 syndrome: Does thymus incidental surgical resection affect its immunological profile? | Coautor: Morán-Barroso V.F., Navarrete-Rodríguez E.M., Del-Rio-Navarro B.E., García-Fajardo D.E., et al. | 2019 | ALLERGOLOGIA ET IMMUNOPATHOLOGIA | WoS-id: 000459947900006
Scopus-id: 2-s2.0-85054138198
| 0 | 0 |
| 8 | Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population | Coautor: Morán-Barroso V.F., Ceron-Rodriguez, Magdalena, Vázquez-Martínez E.R., Garcia-Delgado, Constanza, et al. | 2019 | Annals Of Hepatology | WoS-id: 000483461300014
Scopus-id: 2-s2.0-85069235758
| 9 | 11 |
| 9 | 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 | Coautor: Morán-Barroso V.F., Gómez-Laguna L., Martínez-Herrera A., Reyes-de la Rosa A.D.P., et al. | 2018 | OPHTHALMIC GENETICS | WoS-id: 000428520500011
Scopus-id: 2-s2.0-85029587680
| 6 | 7 |
| 10 | Síndrome de Pallister-Killian en una paciente mestiza mexicana. Reporte de caso | Coautor: Morán-Barroso V.F., Mendelsberg-Fishbein P., Garciá-Delgado C., Munõz-Martinez L.B., et al. | 2018 | ARCHIVOS ARGENTINOS DE PEDIATRIA | WoS-id: 000428743500037
Scopus-id: 2-s2.0-85042009634
| 0 | 0 |
| 11 | Monosomy 9p24 in two non-related patients as result of a translocation (2;9) | Coautor: Moran Barroso, Veronica F., Leon-Carlos, Nayla Y., Garcia-Delgado, Constanza, Morales-Jimenez, Ariadna B., et al. | 2018 | ARCHIVOS ARGENTINOS DE PEDIATRIA | WoS-id: 000439814600026
Scopus-id: 2-s2.0-85051330739
| 1 | 2 |
| 12 | Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature | Coautor: Morán-Barroso V.F., Pastrana-Ayala R., Peña-Castro G.L., Valencia-Herrera A.M., et al. | 2017 | INTERNATIONAL JOURNAL OF DERMATOLOGY | WoS-id: 000397580500024
Scopus-id: 2-s2.0-85013472932
| 4 | 3 |
| 13 | Congenital macroglossia: clinical features and therapeutic strategies in paediatric patients | Coautor: Morán-Barroso, V.F., Núñez-Martínez, P.M., García-Delgado, C., Jasso-Gutiérrez, L. | 2016 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | WoS-id: 000414320000009
Scopus-id: 2-s2.0-84982171739
| 1 | 3 |
| 14 | Caudal duplication with multicystic dysplastic kidney: A case report | Coautor: Morán-Barroso V.F., García-Delgado C., Mendelsberg-Fishbein P., González-Ledón F., et al. | 2015 | CLINICAL DYSMORPHOLOGY | WoS-id: 000346160700007
Scopus-id: 2-s2.0-84918573624
| 1 | 1 |
| 15 | Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease | Coautor: Morán-Barroso V.F., Márquez-Ávila C.S., Vizcaíno-Alarcón A., García-Delgado C., et al. | 2015 | INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | WoS-id: 000363069700020
Scopus-id: 2-s2.0-84952636872
| 8 | 7 |
| 16 | Left cerebral hemisphere and ventricular system abnormalities in a Mexican Meier Gorlin syndrome patient: Widening the clinical spectrum | Coautor: Morán-Barroso V.F., Martínez-Barrera L.E., García-Delgado C., Manzano-Sierra C. | 2014 | GENET COUNSEL | WoS-id: 000338752600009
Scopus-id: 2-s2.0-84904264169
| 1 | 1 |
| 17 | Escobar syndrome with heterotaxia and esophageal atresia: Case report | 2ᵒ autor: Morán-Barroso V.F., Martínez-Barrera L.E., Perezpeña-Díazconti M., Zúñiga-Rodríguez F.G., et al. | 2014 | GENET COUNSEL | WoS-id: 000343073900010
Scopus-id: 2-s2.0-84908164024
| 0 | 1 |
| 18 | Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population | Coautor: Morán-Barroso V.F., Vázquez-Martínez E.R., Varela-Fascinetto G., García-Delgado C., et al. | 2014 | Meta Gene | Scopus-id: 2-s2.0-84901783329
| 0 | 8 |
| 19 | 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 | Coautor: Morán-Barroso V.F., Galaz-Montoya C.I., García-Delgado C., Cervantes-Peredo A., et al. | 2014 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84934755757
| 0 | 1 |
| 20 | Microtia-atresia: Aspectos clínicos, genéticos y genómicos | Coautor: Morán-Barroso V.F., Aguinaga-Ríos M., Frías S., Arenas-Aranda D.J. | 2014 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84938081632
| 0 | 2 |
| 21 | Importance of the diagnosis of protein connexin 26 mutations in the integral management of non-syndromic congenital deafness | Coautor: Morán-Barroso V.F., Mendelsberg-Fishbein P., Márquez-Ávila C.S., García-Delgado C., et al. | 2013 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84877148716
| 0 | 3 |
| 22 | Clinical profile of a patient cohort with Beckwith-Wiedemann syndrome treated at the hospital Infantil de México Federico Gómez (2007 to 2012) | Coautor: Morán-Barroso V.F., Moreno-Salgado R., García-Delgado C., Cervantes-Peredo A., et al. | 2013 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84877156230
| 0 | 4 |
| 23 | Frequency of mucopolysaccharidoses diseases at the Hospital Infantil de Mexico Federico Gomez | Coautor: Morán-Barroso V.F., Fuentes-Fuentes G., Abreu-González M., Gamboa-Marrufo J.D., et al. | 2012 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000209020200010
Scopus-id: 2-s2.0-84874801745
| 0 | 0 |
| 24 | Dermatologic manifestations of Alagille syndrome | Coautor: Barroso V.M., Martínez A.M., Cedillos C.A.M., Zermeño J.N., et al. | 2012 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84865120353
| 0 | 4 |
| 25 | II. Clinical aspects in craniosynostosis [II. Aspectos clínicos en craneosinostosis] | 2ᵒ autor y autor de correspondencia: Morán-Barroso V.F., Saavedra-Ontiveros M.D. | 2003 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0037669849
| 0 | 1 |
| 26 | Oral-facial-digital (OFD) syndrome with associated features: A new syndrome or genetic heterogeneity and variability? | 1ᵉʳ autor: Morân-Barroso V., Valdés Flores M., Garcia-Cavazos R., Kofman-Alfaro S., et al. | 1998 | CLINICAL DYSMORPHOLOGY | WoS-id: 000071513300010
Scopus-id: 2-s2.0-15644367437
| 14 | 17 |
ID's SCOPUS 