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Genetics in Medicine Open
(Jan 2024)
P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants
Leda Torres,
Pedro Reyes,
Benilde García-de Teresa,
María Teresa Villarreal Molina,
Ulises Juárez,
Angélica Solis,
Moises Fiesco-Roa,
Fernando Pérez Villatoro,
Bertha Molina,
Alfredo Rodríguez,
Alessandra Carnevale,
Sara Frías
Affiliations
Leda Torres
Instituto Nacional de Pediatría
Pedro Reyes
Instituto Nacional de Pediatría
Benilde García-de Teresa
Instituto Nacional de Pediatría
María Teresa Villarreal Molina
Instituto Nacional de Medicina Genómica
Ulises Juárez
Instituto Nacional de Pediatría
Angélica Solis
Instituto Nacional de Pediatría
Moises Fiesco-Roa
Instituto Nacional de Pediatría
Fernando Pérez Villatoro
Instituto Nacional de Pediatría
Bertha Molina
Instituto Nacional de Pediatría
Alfredo Rodríguez
Instituto de Investigaciones Biomédicas
Alessandra Carnevale
Instituto Nacional de Medicina Genómica
Sara Frías
Instituto Nacional de Pediatría, Instituto de Investigaciones Biomédicas
Journal volume & issue
Vol. 2
p. 101564
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