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Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
Corona-Rivera, Jorge Román; Corona-Rivera, Alfredo; Zepeda-Romero, Luz Consuelo; Rios-Flores, Izabel Maryalexandra; Rivera-Vargas, Jehú; Orozco-Vela, Mireya; Santana-Bejarano, Uriel Francisco; Torres-Anguiano, Elizabeth; Pinto-Cardoso, Manuela; David, Dezso; Bobadilla-Morales, Lucina.
Afiliação
  • 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.
  • Corona-Rivera A; '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; 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.
  • Rios-Flores IM; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
  • Rivera-Vargas J; Service of Ophthalmology, Division of Pediatrics, 'Fray Antonio Alcalde' Civil Hospital of Guadalajara, Guadalajara, Mexico.
  • Orozco-Vela M; 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.
  • Santana-Bejarano UF; 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.
  • 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; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
  • David D; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
  • Bobadilla-Morales L; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Congenit Anom (Kyoto) ; 59(5): 174-178, 2019 Sep.
Article em En | MEDLINE | ID: mdl-30225942
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades do Olho / Deleção de Genes / Transtornos Cromossômicos / Fatores de Transcrição Forkhead Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: Congenit Anom (Kyoto) Assunto da revista: TERATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: México
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades do Olho / Deleção de Genes / Transtornos Cromossômicos / Fatores de Transcrição Forkhead Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Newborn Idioma: En Revista: Congenit Anom (Kyoto) Assunto da revista: TERATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: México