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MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.
Corona-Rivera, Jorge Román; Zenteno, Juan Carlos; Ordoñez-Labastida, Vianey; Cruz-Cruz, Jessica Paola; Cortés-Pastrana, Rocío Carolina; Peña-Padilla, Christian; Bobadilla-Morales, Lucina; Corona-Rivera, Alfredo; Martínez-Herrera, Alejandro.
Afiliación
  • Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology
  • Zenteno JC; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico; Faculty of Medicine, Department of Biochemistry, UNAM, Mexico City, Mexico; Rare Disease Diagnostic Unit, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.
  • Ordoñez-Labastida V; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico; Rare Disease Diagnostic Unit, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico; Faculty of Medicine, Autonomous University of the State of Morelos (UAEM), Morelos,
  • Cruz-Cruz JP; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico.
  • Cortés-Pastrana RC; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
  • Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
  • Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology
  • Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology
  • Martínez-Herrera A; Rare Disease Diagnostic Unit, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.
Eur J Med Genet ; 66(10): 104826, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37657631
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastornos del Neurodesarrollo / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Trastornos del Neurodesarrollo / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Año: 2023 Tipo del documento: Article