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Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.

Autor: Corona-Rivera JR; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Corona-Rivera A; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Zepeda-Romero LC; Service of Ophthalmology, Division of Pediatrics, 'Fray Antonio Alcalde' Civil Hospital of Guadalajara, Guadalajara, Mexico., Rios-Flores IM; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico., Rivera-Vargas J; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Orozco-Vela M; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Santana-Bejarano UF; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Torres-Anguiano E; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico., Pinto-Cardoso M; Department of Human Genetics, National Health Institute Doutor Ricardo Jorge, Lisbon, Portugal., David D; Department of Human Genetics, National Health Institute Doutor Ricardo Jorge, Lisbon, Portugal., Bobadilla-Morales L; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.

Publikováno v: Congenital anomalies [Congenit Anom (Kyoto)] 2019 Sep; Vol. 59 (5), pp. 174-178. Date of Electronic Publication: 2018 Oct 09.