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Axenfeld-Rieger syndrome: more than meets the eye.
Reis, Linda M; Maheshwari, Mohit; Capasso, Jenina; Atilla, Huban; Dudakova, Lubica; Thompson, Samuel; Zitano, Lia; Lay-Son, Guillermo; Lowry, R Brian; Black, Jennifer; Lee, Joseph; Shue, Ann; Kremlikova Pourova, Radka; Vaneckova, Manuela; Skalicka, Pavlina; Jedlickova, Jana; Trkova, Marie; Williams, Bradley; Richard, Gabriele; Bachman, Kristine; Seeley, Andrea H; Costakos, Deborah; Glaser, Thomas M; Levin, Alex V; Liskova, Petra; Murray, Jeffrey C; Semina, Elena V.
Afiliación
  • Reis LM; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, Wisconsin, USA.
  • Maheshwari M; Department of Pediatric Radiology, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, Wisconsin, USA.
  • Capasso J; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Golisano Children's Hospital and University of Rochester, Rochester, New York, USA.
  • Atilla H; Department of Ophthalmology, School of Medicine, Ankara University, Ankara, Turkey.
  • Dudakova L; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Thompson S; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Wisconsin, Milwaukee, Wisconsin, USA.
  • Zitano L; Department of Medical Genetics, Spectrum Health, Grand Rapids, Michigan, USA.
  • Lay-Son G; Unidad de Genética, División de Pediatría, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Lowry RB; Department of Clinical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Black J; Center for Development, Behavior, and Genetics, SUNY Upstate Medical University, Syracuse, New York, USA.
  • Lee J; Department of Family Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Shue A; Byers Eye Institute, Department of Ophthalmology, Stanford University and Stanford Children's Health, Stanford, California, USA.
  • Kremlikova Pourova R; Department of Biology and Medical Genetics, Second Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Vaneckova M; Department of Radiology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Skalicka P; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Jedlickova J; Department of Ophthalmology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Trkova M; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Williams B; Gennet, Centre for Fetal Medicine and Reproductive Genetics, Prague, Czech Republic.
  • Richard G; GeneDx, Gaithersburg, Maryland, USA.
  • Bachman K; GeneDx, Gaithersburg, Maryland, USA.
  • Seeley AH; Department of Pediatrics, Geisinger Medical Center, Danville, Pennsylvania, USA.
  • Costakos D; Department of Pediatrics, Geisinger Medical Center, Danville, Pennsylvania, USA.
  • Glaser TM; Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Levin AV; Department of Cell Biology and Human Anatomy, UC-Davis School of Medicine, Davis, California, USA.
  • Liskova P; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Golisano Children's Hospital and University of Rochester, Rochester, New York, USA.
  • Murray JC; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Semina EV; Department of Pediatrics, University of Iowa, Iowa City, Iowa, USA.
J Med Genet ; 60(4): 368-379, 2023 04.
Article en En | MEDLINE | ID: mdl-35882526
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías del Ojo / Proteínas de Homeodominio Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías del Ojo / Proteínas de Homeodominio Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido