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Crouzon with acanthosis nigricans. Further delineation of the syndrome L Arnaud‐López, R Fragoso, J Mantilla‐Capacho, P Barros‐Núñez Clinical genetics 72 (5), 405-410, 2007 | 77 | 2007 |
Novel hairless mutations in two kindreds with autosomal recessive papular atrichia R Kruse, S Cichon, M Anker, AM Hillmer, P Barros-Núñez, JM Cantú, ... Journal of investigative dermatology 113 (6), 954-959, 1999 | 73 | 1999 |
Wnt-â-catenina signaling pathway and its relationship with cancer AB Ochoa-Hernández, CI Juárez-Vázquez, MA Rosales-Reynoso, ... Cirugia y cirujanos 80 (4), 389-398, 2012 | 44 | 2012 |
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene. JM Mantilla-Capacho, L Arnaud, M Diaz-Rodriguez, P Barros-Nunez Genetic Counseling (Geneva, Switzerland) 16 (4), 403-406, 2005 | 42 | 2005 |
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Peripheral T-lymphocytes express WNT7A and its restoration in leukemia-derived lymphoblasts inhibits cell proliferation AB Ochoa-Hernández, M Ramos-Solano, ID Meza-Canales, ... BMC cancer 12, 1-18, 2012 | 31 | 2012 |
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MHC class I-related chain A and B ligands are differentially expressed in human cervical cancer cell lines S del Toro-Arreola, N Arreygue-Garcia, A Aguilar-Lemarroy, A Cid-Arregui, ... Cancer cell international 11, 1-10, 2011 | 30 | 2011 |
Gene expression profiling identifies WNT7A as a possible candidate gene for decreased cancer risk in fragile X syndrome patients MA Rosales-Reynoso, AB Ochoa-Hernández, A Aguilar-Lemarroy, ... Archives of medical research 41 (2), 110-118. e2, 2010 | 30 | 2010 |
Melorheostosis: unusual presentation in a girl RP Mariaud-Schmidt, WE Bitar, F Pérez-Lamero, P Barros-Nuñez Clinical imaging 26 (1), 58-62, 2002 | 29 | 2002 |
Femoral–facial syndrome with malformations in the central nervous system E Leal, N Macı́as-Gómez, L Rodrı́guez, FM Mercado, P Barros-Núñez Clinical imaging 27 (1), 23-26, 2003 | 28 | 2003 |
Hamartoma involving the pseudarthrosis site in patients with neurofibromatosis type 1 RP Mariaud-Schmidt, S Rosales-Quintana, E Bitar, D Fajardo, ... Pediatric and Developmental Pathology 8 (2), 190-196, 2005 | 25 | 2005 |
A novel mutation in CDMP1 causes brachydactyly type C with “angel-shaped phalanx”. A genotype–phenotype correlation in the mutational spectrum BE Gutiérrez-Amavizca, AJL Brambila-Tapia, CI Juárez-Vázquez, ... European journal of medical genetics 55 (11), 611-614, 2012 | 20 | 2012 |
Evolución y genómica del cerebro humano MA Rosales-Reynoso, CI Juárez-Vázquez, P Barros-Núñez Neurologia 33 (4), 254-265, 2018 | 19 | 2018 |
Evolution and genomics of the human brain MA Rosales-Reynoso, CI Juárez-Vázquez, P Barros-Núñez Neurología (English Edition) 33 (4), 254-265, 2018 | 19 | 2018 |