| Liver disease in pregnancy: Medical aspects and their implications for mother and child CS García-Romero, C Guzman, A Cervantes, M Cerbón Annals of hepatology 18 (4), 553-562, 2019 | 93 | 2019 |
| Cytogenetic profile in 1,921 cases of trisomy 21 syndrome F Flores-Ramírez, C Palacios-Guerrero, C García-Delgado, ... Archives of medical research 46 (6), 484-489, 2015 | 62 | 2015 |
| A mutation in the 5′ non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism P Canto, E de la Chesnaye, M López, A Cervantes, B Chávez, F Vilchis, ... The Journal of Clinical Endocrinology & Metabolism 85 (5), 1908-1911, 2000 | 59 | 2000 |
| Metilación del ADN: un fenómeno epigenético de importancia médica M Rodríguez Dorantes, N Téllez Ascencio, MA Cerbón, M López, ... Revista de investigación clínica 56 (1), 56-71, 2004 | 58 | 2004 |
| Frequency of Y chromosomal material in Mexican patients with Ullrich‐Turner syndrome M López, P Canto, M Aguinaga, L Torres, A Cervantes, G Alfaro, ... American journal of medical genetics 76 (2), 120-124, 1998 | 56 | 1998 |
| Clinical traits and molecular findings in 46, XX males M López, L Torres, JP Méndez, A Cervantes, G Pérez‐Palacios, ... Clinical genetics 48 (1), 29-34, 1995 | 48 | 1995 |
| Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes N Monroy, M López, A Cervantes, D García‐Cruz, G Zafra, S Canún, ... American journal of medical genetics 107 (3), 181-189, 2002 | 47 | 2002 |
| Persistence of decidual NK cells and KIR genotypes in healthy pregnant and preeclamptic women: a case-control study in the third trimester of gestation EN Sánchez-Rodríguez, S Nava-Salazar, CA Mendoza-Rodríguez, ... Reproductive Biology and Endocrinology 9, 1-9, 2011 | 37 | 2011 |
| DNA methylation: an epigenetic process of medical importance M Rodríguez Dorantes, N Téllez Ascencio, MA Cerbón, M López, ... Revista de investigacion clinica 56 (1), 56-71, 2004 | 35 | 2004 |
| Prevalencia de mosaicismo para la trisomía 21 y análisis de las variantes citogenéticas en pacientes con diagnóstico de síndrome de Down: Revisión de 24 años (1986-2010) del … LM Garduño-Zarazúa, L Giammatteo Alois, S Kofman-Epstein, ... Boletín médico del Hospital infantil de México 70 (1), 31-36, 2013 | 34 | 2013 |
| Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes L Torres, M López, JP Méndez, P Canto, A Cervantes, G Alfaro, ... American journal of medical genetics 63 (2), 348-355, 1996 | 23 | 1996 |
| SRY alone can induce normal male sexual differentiation M López, L Torres, JP Méndez, A Cervantes, G Alfaro, G Pérez‐Palacios, ... American journal of medical genetics 55 (3), 356-358, 1995 | 23 | 1995 |
| Clinical, cytogenetic, and biochemical analyses of a family with at (3; 13)(q26. 2; p11. 2): further delineation of 3q duplication syndrome M Abreu-González, C García-Delgado, A Cervantes, A Aparicio-Onofre, ... Case Reports in Genetics 2013, 2013 | 20 | 2013 |
| PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype A Cervantes, R Guevara‐Yáñez, M López, N Monroy, M Aguinaga, ... Clinical genetics 60 (5), 385-392, 2001 | 19 | 2001 |
| 19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype C Venegas-Vega, K Nieto-Martínez, A Martínez-Herrera, ... Molecular Cytogenetics 7, 1-7, 2014 | 16 | 2014 |
| Cytogenetic findings in 303 Mexican patients with de novo acute myeloblastic leukemia. RM Arana-Trejo, E Gómez-Morales, ME Rubio-Borja, JJ Kassack-Ipiña, ... Archives of medical research 28 (2), 209-214, 1997 | 14 | 1997 |
| Importancia del diagnóstico de mutaciones en el gen de la conexina 26 en el manejo integral de la sordera congénita no sindrómica P Mendelsberg-Fishbein, CS Márquez-Ávila, C García-Delgado, ... Boletín Médico del Hospital Infantil de México 70 (2), 89-97, 2013 | 12 | 2013 |
| Body mass index implications in intrahepatic cholestasis of pregnancy and placental histopathological alterations V Valdovinos-Bello, CS García-Romero, A Cervantes-Peredo, ... Annals of Hepatology 28 (1), 100879, 2023 | 9 | 2023 |
| Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population M Cerón-Rodríguez, ER Vázquez-Martínez, C García-Delgado, ... Annals of Hepatology 18 (4), 613-619, 2019 | 9 | 2019 |
| Prevalence of mosaicism for trisomy 21 and cytogenetic variant analysis in patients with clinical diagnosis of Down syndrome: a 24-year review (1986-2010) at the Servicio de … LM Garduño-Zarazúa, LG Alois, S Kofman-Epstein, ABC Peredo Boletín médico del Hospital Infantil de México 70 (1), 31-37, 2013 | 9 | 2013 |
Susana Kofman AlfaroProfesor titutlar BVerified email at unam.mx
