Deciphering the etiology of undiagnosed ocular anomalies along with systemic alterations in pediatric patients through whole exome sequencing
Reyna-Fabián, Miriam E., Fernández-Hernández, Liliana, Enríquez-Flores, Sergio, Apam-Garduño, David, Prado-Larrea, Carolina, Seo, Go Hun, Khang, Rin, Cortés-González, Vianney
Published in Scientific reports (22.06.2024)
Published in Scientific reports (22.06.2024)
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Journal Article
TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant
Reyna-Fabián, Miriam E., Alcántara-Ortigoza, Miguel A., Hernández-Martínez, Nancy L., Berumen, Jaime, Jiménez-García, Raquel, Gómez-Garza, Gilberto, González-del Angel, Ariadna
Published in Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia (01.01.2020)
Published in Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia (01.01.2020)
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Journal Article
Detecting a Complex of Cryptic Species within Neoechinorhynchus golvani (Acanthocephala: Neoechinorhynchidae) Inferred from ITSs and LSU rDNA Gene Sequences
Martínez-Aquino, Andrés, Reyna-Fabián, Miriam E, Rosas-Valdez, Rogelio, Razo-Mendivil, Ulises, de León, Gerardo Pérez-Ponce, García-Varela, Martín
Published in The Journal of parasitology (01.10.2009)
Published in The Journal of parasitology (01.10.2009)
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Journal Article
Validating the systematic position of Plationus Segers, Murugan & Dumont, 1993 (Rotifera: Brachionidae) using sequences of the large subunit of the nuclear ribosomal DNA and of cytochrome C oxidase
Reyna-Fabián, Miriam E, Laclette, Juan Pedro, Cummings, Michael P, García-Varela, Martín
Published in Hydrobiologia (01.05.2010)
Published in Hydrobiologia (01.05.2010)
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Journal Article
First comprehensive TSC1/TSC2 mutational analysis in Mexican patients with Tuberous Sclerosis Complex reveals numerous novel pathogenic variants
Reyna-Fabián, Miriam E., Hernández-Martínez, Nancy L., Alcántara-Ortigoza, Miguel A., Ayala-Sumuano, Jorge T., Enríquez-Flores, Sergio, Velázquez-Aragón, José A., Varela-Echavarría, Alfredo, Todd-Quiñones, Carlos G., González-del Angel, Ariadna
Published in Scientific reports (20.04.2020)
Published in Scientific reports (20.04.2020)
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Journal Article
Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate
Velázquez-Aragón, José A, González-Del Angel, Ariadna, Alcántara-Ortigoza, Miguel A, Reyna-Fabián, Miriam E, Estandia-Ortega, Bernardette
Published in The Cleft palate-craniofacial journal (01.09.2021)
Published in The Cleft palate-craniofacial journal (01.09.2021)
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Journal Article
Analysis of the Bacterial Diversity in Liver Abscess: Differences Between Pyogenic and Amebic Abscesses
Reyna-Fabián, Miriam E, Zermeño, Valeria, Ximénez, Cecilia, Flores, Janin, Romero, Miguel F, Diaz, Daniel, Argueta, Jesús, Moran, Patricia, Valadez, Alicia, Cerritos, René
Published in The American journal of tropical medicine and hygiene (01.01.2016)
Published in The American journal of tropical medicine and hygiene (01.01.2016)
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Journal Article
Association of interactions among the IRF6 gene, the 8q24 region, and maternal folic acid intake with non-syndromic cleft lip/palate in Mexican Mestizos
Velazquez-Aragon, José A, Alcantara-Ortigoza, Miguel A, Estandia-Ortega, Bernardette, Reyna-Fabian, Miriam E, Cruz-Fuentes, Carlos, Villagomez, Sandra, Gonzalez-del Angel, Ariadna
Published in American journal of medical genetics. Part A (01.12.2012)
Published in American journal of medical genetics. Part A (01.12.2012)
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Journal Article
5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate
Estandia-Ortega, Bernardette, Velázquez-Aragón, José A., Alcántara-Ortigoza, Miguel A., Reyna-Fabian, Miriam E., Villagómez-Martínez, Sandra, González-del Angel, Ariadna
Published in European journal of oral sciences (01.04.2014)
Published in European journal of oral sciences (01.04.2014)
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Journal Article
Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects
Alcántara-Ortigoza, Miguel A., De Rubens-Figueroa, Jesús, Reyna-Fabian, Miriam E., Estandía-Ortega, Bernardette, González-del Angel, Ariadna, Molina-Álvarez, Bertha, Velázquez-Aragón, José A., Villagómez-Martínez, Sandra, Pereira-López, Gabriela I., Martínez-Cruz, Víctor, Álvarez-Gómez, Rosa M., Díaz-García, Luisa
Published in Pediatric cardiology (01.10.2015)
Published in Pediatric cardiology (01.10.2015)
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Journal Article
Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects
Alcántara-Ortigoza, Miguel A., De Rubens-Figueroa, Jesús, Reyna-Fabian, Miriam E., Estandía-Ortega, Bernardette, González-del Angel, Ariadna, Molina-Álvarez, Bertha, Velázquez-Aragón, José A., Villagómez-Martínez, Sandra, Pereira-López, Gabriela I., Cruz-Martínez, Víctor, Álvarez-Gómez, Rosa M., García-Díaz, Luisa
Published in Pediatric cardiology (01.04.2015)
Published in Pediatric cardiology (01.04.2015)
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Journal Article
TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant
Reyna-Fabián, Miriam E., Alcántara-Ortigoza, Miguel A., Hernández-Martínez, Nancy L., Berumen, Jaime, Jiménez-García, Raquel, Gómez-Garza, Gilberto, González-del Angel, Ariadna
Published in Nefrología (01.01.2020)
Published in Nefrología (01.01.2020)
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Journal Article
TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant
Miriam E. Reyna-Fabián, Miguel A. Alcántara-Ortigoza, Nancy L. Hernández-Martínez, Jaime Berumen, Raquel Jiménez-García, Gilberto Gómez-Garza, Ariadna González-del Angel
Published in Nefrología (01.01.2020)
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Published in Nefrología (01.01.2020)
Journal Article