Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy
Ramos, Sandra, Navarrete‐Meneses, Pilar, Molina, Bertha, Cervantes‐Barragán, David E., Lozano, Valentn, Gallardo, Emma, Marchetti, Francesco, Frias, Sara
Published in Environmental and molecular mutagenesis (01.10.2018)
Published in Environmental and molecular mutagenesis (01.10.2018)
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Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome
Nakamura, Kazuyuki, Kato, Mitsuhiro, Osaka, Hitoshi, Yamashita, Sumimasa, Nakagawa, Eiji, Haginoya, Kazuhiro, Tohyama, Jun, Okuda, Mitsuko, Wada, Takahito, Shimakawa, Shuichi, Imai, Katsumi, Takeshita, Saoko, Ishiwata, Hisako, Lev, Dorit, Lerman-Sagie, Tally, Cervantes-Barragán, David E, Villarroel, Camilo E, Ohfu, Masaharu, Writzl, Karin, Gnidovec Strazisar, Barbara, Hirabayashi, Shinichi, Chitayat, David, Myles Reid, Diane, Nishiyama, Kiyomi, Kodera, Hirofumi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Hayasaka, Kiyoshi, Matsumoto, Naomichi, Saitsu, Hirotomo
Published in Neurology (10.09.2013)
Published in Neurology (10.09.2013)
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Editing the Human Genome with CRISPR/Cas: A Review of its Molecular Basis, Current Clinical Applications, and Bioethical Implications
Ahumada-Ayala, Miguel, Aguilar-López, Regina, González-Stoylov, Nicolai, Palacio-Sosa, Esmeralda, Cervantes-Barragán, David E, Fernández-Hernández, Liliana
Published in Revista de investigacion clinica (01.01.2023)
Published in Revista de investigacion clinica (01.01.2023)
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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
Cervantes-Barragán, David E, Villarroel, Camilo E, Medrano-Hernández, Alma, Durán-McKinster, Carola, Bosch-Canto, Vanessa, del-Castillo, Victoria, Nazarenko, Irina, Yang, Amy, Desnick, Robert J
Published in Journal of medical genetics (01.10.2011)
Published in Journal of medical genetics (01.10.2011)
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Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7
Salas-Labadía, Consuelo, Cervantes-Barragán, David E., Cruz-Alcívar, Roberto, Daber, Robert D., Conlin, Laura K., Leonard, Laura D., Spinner, Nancy B., Durán-McKinster, Carola, Dávila-Ortíz de Montellano, David J., Del Castillo-Ruiz, Victoria, Pérez-Vera, Patricia
Published in American journal of medical genetics. Part A (01.07.2014)
Published in American journal of medical genetics. Part A (01.07.2014)
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Clinical heterogeneity in Andersen-Tawil syndrome
Totomoch-Serra, Armando, Márquez, Manlio F., Cervantes-Barragan, David E.
Published in Neuromuscular disorders : NMD (01.11.2017)
Published in Neuromuscular disorders : NMD (01.11.2017)
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Pediatric Porcelain Aorta Secondary to Gaucher Disease Type 3C With Successful Aortic Replacement Surgery
Silva-Estrada, Jorge, Cervantes-Barragán, David E., Reyes-de la Cruz, Lorenzo, Meléndez-Ramírez, Gabriela, Meave, Aloha, Alaez-Verson, Carmen
Published in JACC. Case reports (16.11.2022)
Published in JACC. Case reports (16.11.2022)
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Journal Article
Pediatric Porcelain Aorta Secondary to Gaucher Disease Type 3C With Successful Aortic Replacement Surgery
Silva-Estrada, Jorge, Cervantes-Barragán, David E, Reyes-de la Cruz, Lorenzo, Meléndez-Ramírez, Gabriela, Meave, Aloha, Alaez-Verson, Carmen
Published in JACC. Case reports (16.11.2022)
Published in JACC. Case reports (16.11.2022)
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