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Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome

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第一作者: Disciglio,V.
作者单位: Department of Clinical Genetics, Alder Hey Children's Hospital, Liverpool, and Liverpool Women's [1] Laboratory of Genetic Diagnosis, IRCCS Associazione Oasi Maria Santissima, Troina, Italy, Medical [2] Department of Molecular Medicine and Surgery, CMM, Karolinska Institutet, Hospital Stockholm, Sweden [3] Institut de Génétique Médicale, H?pital Jeanne de Flandre, Lille, France [4] Manchester Academic Health Sciences Centre, Manchester Biomedical Research Centre, St Mary's [5] Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy [6] Medical Genetics, University of Siena, Siena, Italy, Genetica Medica, Azienda Ospedaliera [7] Dipartimento di Pediatria, Ospedale Valdichiana, Montepulciano, Italy [8] Department of Developmental Neuroscience, IRCCS Stella Maris, Calambrone, Italy [9] Unit of Pediatrics and Medical Genetics, IRCCS Associazione Oasi Maria Santissima, Troina, Italy [10] Service de Génétique Clinique, H?pital Jeanne de Flandre, Lille, France [11] Medical Genetics, Institute for Maternal and Child Health IRCCS Burlo Garofalo, Trieste, Italy [12] Medical Genetics, University of Siena, Siena, Italy [13] IRCCS Casa Sollievo della Sofferenza Hospital, Mendel Institute, Rome, Italy [14] CHU Nantes, Service de genetique medicale, Nantes Cedex, France [15]
发布时间 2015-03-11
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American journal of medical genetics, Part A

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