| DEB test for Fanconi anemia detection in patients with atypical phenotypes C Esmer, S Sanchez, S Ramos, B Molina, S Frias, A Carnevale American Journal of Medical Genetics Part A 124 (1), 35-39, 2004 | 76 | 2004 |
| Nonclonal chromosome aberrations and genome chaos in somatic and germ cells from patients and survivors of hodgkin lymphoma S Frias, S Ramos, C Salas, B Molina, S Sánchez, R Rivera-Luna Genes 10 (1), 37, 2019 | 32 | 2019 |
| Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring S Frias, S Ramos, B Molina, V del Castillo, DG Mayén Mutation Research/Genetic Toxicology and Environmental Mutagenesis 520 (1-2 …, 2002 | 31 | 2002 |
| Local and circulating microchimerism is associated with hypersensitivity pneumonitis ML Bustos, S Frías, S Ramos, A Estrada, JL Arreola, F Mendoza, ... American journal of respiratory and critical care medicine 176 (1), 90-95, 2007 | 30 | 2007 |
| Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors FS Salas C, Niembro A, Lozano V, Gallardo E, Molina B, Sánchez S, Ramos S ... Environ Mol Mutagen 53 (4), 271-80, 2012 | 26 | 2012 |
| Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy S Ramos, P Navarrete‐Meneses, B Molina, DE Cervantes‐Barragán, ... Environmental and Molecular Mutagenesis 59 (8), 755-768, 2018 | 17 | 2018 |
| Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics E Yokoyama, V Del Castillo, S Sánchez, S Ramos, B Molina, L Torres, ... Molecular Cytogenetics 11, 1-8, 2018 | 11 | 2018 |
| Acrocentric cryptic translocation associated with nondisjunction of chromosome 21 S Ramos, MA Alcántara, B Molina, V del Castillo, S Sánchez, S Frias American Journal of Medical Genetics Part A 146 (1), 97-102, 2008 | 9 | 2008 |
| Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in F anconi anemia cells B Molina, F Marchetti, L Gómez, S Ramos, L Torres, R Ortiz, ... Environmental and Molecular Mutagenesis 56 (5), 457-467, 2015 | 8 | 2015 |
| Primeros casos de monosomía 1p36 en México: diagnóstico a considerar en pacientes con retraso mental y dismorfas CE Villarroel, RM Álvarez, L Gómez-Laguna, S Ramos, GD Ángela Archivos argentinos de pediatría 109 (3), e55-e58, 2011 | 5 | 2011 |
| Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples S Ramos, R Rodríguez, O Castro, P Grether, B Molina, S Frias International Journal of Molecular Sciences 20 (21), 5251, 2019 | 3 | 2019 |
| Unique association of hypochondroplasia with craniosynostosis and cleft palate in a Mexican family A González‐del Angel, A Caro‐Contreras, MA Alcántara‐Ortigoza, ... American Journal of Medical Genetics Part A 176 (1), 161-166, 2018 | 3 | 2018 |
| First two Mexican cases of monosomy 1p36: possible diagnosis in patients with mental retardation and dysmorphism CE Villarroel, RM Alvarez, L Gomez-Laguna, S Ramos, ... Archivos Argentinos de Pediatria 109 (3), e55-8, 2011 | 2 | 2011 |
| Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide S Ramos, B Molina, P Grether, DG Mayén, O Castro, M Ángeles, ... Acta pediátrica de México 36 (5), 374-382, 2015 | 1 | 2015 |
| Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case A Martínez, S Ramos, AG Angel, MÁ Alcántara, B Molina, A Carnevale Revista de Investigación Clínica 59 (6), 444, 2007 | 1 | 2007 |
| REPORT OF A PATIENT WITH A DE NOVO NON-RECURRENT DUPLICATION OF 17P11.2P12 AND YQ11 DELETION GDELAA INICIAL PAG. FINAL GRUPO AREA CONCURSA FERNÁNDEZ-HERNÁNDEZ LILIANA ... Mol Cytogen 12 (35), 1-8, 2019 | | 2019 |
| Genomic chaos in peripheral blood lymphocytes of hodgkins lymphoma patients 1 year after ABVD chemotherapy/radiotherapy (vol 60, pg 387, 2019) S Frias, S Ramos, B Molina ENVIRONMENTAL AND MOLECULAR MUTAGENESIS 60 (6), 563-563, 2019 | | 2019 |
| Corrigendum to “Genomic chaos in peripheral blood lymphocytes of hodgkins lymphoma patients1 year after ABVD chemotherapy/radiotherapy” S Frias, INP Laboratorio de Citogenética, I Sur, S Frias, S Ramos, ... Environmental and Molecular Mutagenesis 60 (563), 2019 | | 2019 |
| OMPHALOCELE, BLADDER EXTROPHY, IMPERFORATE ANUS, SPINE DEFECTS COMPLEX, AND BILATERAL CLEFT LIP AND PALATE IN ONE PRODUCT OF A TRIPLET PREGNANCY OBTAINED BY IN VITRO … GA Yokoyama RE., Del Castillo V., Ramos S. Am J Med Genet A 143, 1933-1995, 2007 | | 2007 |
Sara FriasInstituto Nacional de Pediatria/Instituto de Investigaciones Biomedicas UNAM在 biomedicas.unam.mx 的电子邮件经过验证
