Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cruz-Cruz JP"'
Autor:
Cruz-Cruz JP; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico., Nieto-García R; Service of Cardiology, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico., Rivera-Ramírez PB; Service of Cardiology, Pediatrics 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 Cytogenetics Unit, Pediatrics 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 Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico., Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico., Rodríguez-Machuca VU; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico., Valdez-Muñoz SR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico., Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Publikováno v:
Congenital anomalies [Congenit Anom (Kyoto)] 2025 Jan-Dec; Vol. 65 (1), pp. e12589.
Autor:
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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico. Electronic address: rocorona@cucs.udg.mx., 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, Mexico., 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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico., 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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico., Martínez-Herrera A; Rare Disease Diagnostic Unit, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2023 Oct; Vol. 66 (10), pp. 104826. Date of Electronic Publication: 2023 Aug 30.
Autor:
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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico., Bustos Rodríguez FJ; Service of Pathology, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico., Vega-Silva LL; Service of Dermatology, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico., Hernández-Camarena F; Service of Pathology, 'Fray Antonio Alcalde' 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., Castillo-Reyes KA; 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., 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., 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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico., 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 and Genomics, Health Sciences University Centre, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2023 Jun; Vol. 191 (6), pp. 1669-1671. Date of Electronic Publication: 2023 Mar 18.