| 1 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Del Castillo, Victoria, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 2 | Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review | Coautor: Del Castillo-Ruiz, V, Martinez-Hernandez, A., Martinez-Anaya, D., Duran-McKinster, C., et al. | 2022 | BMC MEDICAL GENOMICS | WoS-id: 000877014900002
Scopus-id: 2-s2.0-85140943693
| 0 | 0 |
| 3 | UPD(14)mat and UPD(14)mat in concomitance with mosaic small supernumerary marker chromosome 14 in two new patients with Temple syndrome | Coautor: Del Castillo-Ruiz V., Garza-Mayén G., Ulloa-Avilés V., Villarroel C.E., et al. | 2021 | EUROPEAN JOURNAL OF MEDICAL GENETICS | Scopus-id: 2-s2.0-85103317977
| 0 | 5 |
| 4 | Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review | Coautor: DEL CASTILLO, VICTORIA, Yokoyama, Emiy, Villarroel, Camilo E., Diaz, Sinhue, et al. | 2020 | MOLECULAR CYTOGENETICS | WoS-id: 000571115500001
Scopus-id: 2-s2.0-85091273525
| 3 | 3 |
| 5 | Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: Revealing the genetic basis of clinical manifestations | Coautor: Del Castillo-Ruiz, V, Salas-Labadia, C., Gomez-Carmona, S., Cruz-Alcivar, R., et al. | 2019 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000497424400002
Scopus-id: 2-s2.0-85075037719
| 17 | 19 |
| 6 | Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics | 2ᵒ autor: Del Castillo V., Yokoyama E., Sánchez S., Ramos S., et al. | 2018 | MOLECULAR CYTOGENETICS | WoS-id: 000431897500002
Scopus-id: 2-s2.0-85046671603
| 5 | 6 |
| 7 | Further delineation of achondroplasia?hypochondroplasia complex with long-term survival | Coautor: del Castillo V., González-del Angel A., Rius R., Alcántara-Ortigoza M.A., et al. | 2018 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000433440600025
Scopus-id: 2-s2.0-85045832498
| 0 | 0 |
| 8 | Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas | Coautor y autor de correspondencia: Del Castllo-Ruiz V., Yokoyama-Rebollar E., FrÃas S. | 2017 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-85040685878
| 0 | 1 |
| 9 | Genómica del síndrome de Down | Coautor y autor de correspondencia: Del Castllo-Ruiz V., Díaz-Cuéllar S., Yokoyama-Rebollar E. | 2016 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-84989914500
| 0 | 8 |
| 10 | Angelman Syndrome due to familial translocation: Unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization | Coautor: Del Castillo-Ruiz V., Yokoyama-Rebollar E., Ruiz-Herrera A., Lieberman-Hernández E., et al. | 2015 | MOLECULAR CYTOGENETICS | WoS-id: 000353104300001
Scopus-id: 2-s2.0-84949127641
| 1 | 1 |
| 11 | Population structure and fecundity in Uca virens Salmon & Atsaides, 1968 (Decapoda: Ocypodidae) in southern Tamiahua Lagoon, Veracruz, Mexico | 1ᵉʳ autor: del Castillo, V, Perez, LL, Alonso, MD, Bortolini, JL | 2015 | LATIN AMERICAN JOURNAL OF AQUATIC RESEARCH | WoS-id: 000353582800002
Scopus-id: 2-s2.0-84927940585
| 2 | 3 |
| 12 | Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7 | Coautor: Del Castillo-Ruiz V., Salas-Labadía C., Cervantes-Barragán D.E., Cruz-Alcívar R., et al. | 2014 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000337633300023
Scopus-id: 2-s2.0-84902548321
| 7 | 7 |
| 13 | Differential distribution of HP1 proteins after trichostatin a treatment influences chromosomal stability in HCT116 and WI-38 cells | Coautor: del Castillo, V, Gonzalez-Barrios, R, Soto-Reyes, E, Quiroz-Baez, R, et al. | 2014 | CELL DIVISION | WoS-id: 000350408800002
Scopus-id: 2-s2.0-84924235901
| 4 | 4 |
| 14 | Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: Review of the focal facial dermal dysplasias and subtype reclassification | Coautor: del-Castillo V., Cervantes-Barragán D.E., Villarroel C.E., Medrano-Hernández A., et al. | 2011 | JOURNAL OF MEDICAL GENETICS | Scopus-id: 2-s2.0-80955136596
| 0 | 26 |
| 15 | Hypomelanosis of Ito: Diagnostic criteria and report of 41 cases | Coautor: del Castillo V., Ruiz-Maldonado R., Toussaint S., Tamayo L., et al. | 1992 | PEDIATRIC DERMATOLOGY | WoS-id: A1992HJ83100001
Scopus-id: 2-s2.0-0026528367
| 103 | 147 |
| 16 | Enfermedad de orina de jarabe de arce: heterogeneidad genética, diagnóstico de heterocigotos y un nuevo enfoque terapéutico. | Coautor: Del Castillo V., Velázquez A., Montiel F., Sahw K.N., et al. | 1981 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1981ME80100005
Scopus-id: 2-s2.0-0019595042
| 1 | 1 |
ID's SCOPUS 