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New patients with Temple syndrome caused by 14q32 deletion: Genotype‐phenotype correlations and risk of thyroid cancer
Authors:Giulia Severi  Laura Bernardini  Silvana Briuglia  Stefania Bigoni  Barbara Buldrini  Pamela Magini  Maria L. Dentici  Duccio M. Cordelli  Teresa Arrigo  Emilio Franzoni  Sergio Fini  Eleonora Italyankina  Italia Loddo  Antonio Novelli  Claudio Graziano
Affiliation:1. Medical Genetics Unit, Policlinico S. Orsola‐Malpighi, University of Bologna, Bologna, Italy;2. IRCCS‐Casa Sollievo della Sofferenza, Mendel Institute, Rome, Italy;3. Department of Pediatrics, University of Messina, Messina, Italy;4. Medical Genetics Unit, Ferrara University Hospital, Ferrara, Italy;5. Medical Genetics Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy;6. Child Neurology Unit, University of Bologna, Bologna, Italy;7. Correspondence to:;8. Claudio Graziano, U.O. Genetica Medica, Policlinico S. Orsola‐Malpighi. Via Massarenti 9, 40138 Bologna, Italy. E‐mail:
Abstract:
Keywords:14q32 deletion  DIO3  DLK1  Temple syndrome  thyroid cancer  YY1
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