Výsledky vyhledávání - "Woerner, Audrey C."

Akademický článek

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

Autor: Kalanithy JC; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany jkalanithy@uni-bonn.de.; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany., Mingardo E; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany., Stegmann JD; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany., Dhakar R; Genome and Computational Biology Lab, Department of Biotechnology, Mohanlal Sukhadia University, Udaipur, Rajasthan, India., Dakal TC; Genome and Computational Biology Lab, Department of Biotechnology, Mohanlal Sukhadia University, Udaipur, Rajasthan, India., Rosenfeld JA; Baylor Genetics Laboratories, Houston, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Tan WH; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts, USA., Coury SA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts, USA.; Genomes2People Research Program, Division of Genetics, Department of Medicine, Mass General Brigham Inc, Boston, Massachusetts, USA., Woerner AC; Department of Pediatrics, Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA., Sebastian J; Department of Pediatrics, Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA., Levy PA; Department of Pediatrics, Children's Hospital at Montefiore, New York, New York, USA., Fleming LR; Genetics and Metabolic Clinic, St Luke's Health System, Boise, Idaho, USA., Waffenschmidt L; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany., Lindenberg TT; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany., Yilmaz Ö; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany., Channab K; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany., Babra BK; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany., Christ A; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany., Eiberger B; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany., Hölzel S; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany.; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany., Vidic C; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany., Häberlein F; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany.; Institute of Pharmaceutical Biology, Molecular, Cellular, and Pharmacobiology Section, University of Bonn, Bonn, Germany., Ishorst N; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany.; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany., Rodriguez-Gatica JE; Clausius Institute of Physical and Theoretical Chemistry, University of Bonn, Bonn, Germany., Pezeshkpoor B; Institute for Experimental Hematology and Transfusion Medicine, University Hospital Bonn, Bonn, Germany.; Center for Rare Diseases Bonn, University Hospital Bonn, Bonn, Germany., Kupczyk PA; Department of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany., Vanakker OM; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Loddo S; Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Novelli A; Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Dentici ML; Medical Genetics Unit, Academic Department of Pediatrics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Becker A; Institute for Cellular Neurosciences II, University Hospital Bonn, Bonn, Germany., Thiele H; Cologne Center for Genomics, University of Cologne, Cologne, Germany., Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Lupski JR; Molecular and Human Genetics; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Hilger AC; Research Center On Rare Kidney Diseases (RECORD), Erlangen University Hospital, Erlangen, Germany.; Department of Pediatrics and Adolescent Medicine, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany., Reutter HM; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.; Department of Pediatric and Adolescent Medicine, Division Neonatology and Pediatric Intensive Care, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Institute of Human Genetics, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany., Merz WM; Department of Obstetrics and Prenatal Medicine, University Hospital Bonn, Bonn, Germany., Dworschak GC; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany.; Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.; Department of Neuropediatrics, University Hospital Bonn, Bonn, Germany., Odermatt B; Institute of Neuroanatomy, Medical Faculty, University of Bonn, Bonn, Germany.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, Bonn, Germany.

Publikováno v: Journal of medical genetics [J Med Genet] 2024 Dec 23. Date of Electronic Publication: 2024 Dec 23.

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