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ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.
Zak, J; Vives, V; Szumska, D; Vernet, A; Schneider, J E; Miller, P; Slee, E A; Joss, S; Lacassie, Y; Chen, E; Escobar, L F; Tucker, M; Aylsworth, A S; Dubbs, H A; Collins, A T; Andrieux, J; Dieux-Coeslier, A; Haberlandt, E; Kotzot, D; Scott, D A; Parker, M J; Zakaria, Z; Choy, Y S; Wieczorek, D; Innes, A M; Jun, K R; Zinner, S; Prin, F; Lygate, C A; Pretorius, P; Rosenfeld, J A; Mohun, T J; Lu, X.
Affiliation
  • Zak J; Ludwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, UK.
  • Vives V; Ludwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, UK.
  • Szumska D; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.
  • Vernet A; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.
  • Schneider JE; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.
  • Miller P; Ludwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, UK.
  • Slee EA; Ludwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, UK.
  • Joss S; Queen Elizabeth University Hospital Glasgow, Glasgow G51 4TF, UK.
  • Lacassie Y; Department of Pediatrics, Louisiana State University, New Orleans, LA 70118, USA.
  • Chen E; Genetics Services, Children's Hospital New Orleans, New Orleans, LA 70118, USA.
  • Escobar LF; Kaiser Permanente, San Francisco Medical Center, San Francisco, CA 94115, USA.
  • Tucker M; St Vincent Children's Hospital, Indianapolis, IN 46260, USA.
  • Aylsworth AS; St Vincent Children's Hospital, Indianapolis, IN 46260, USA.
  • Dubbs HA; Departments of Pediatrics and Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Collins AT; Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Andrieux J; Seattle Children's Hospital, Seattle, WA 98105, USA.
  • Dieux-Coeslier A; Institute of Medical Genetics, Jeanne de Flandre Hospital, CHRU de Lille, Lille 59000, France.
  • Haberlandt E; CHU Lille, Clinique de Génétique, Lille F-59000, France.
  • Kotzot D; Clinical Department of Pediatrics, Innsbruck Medical University, Innsbruck A-6020, Austria.
  • Scott DA; Division of Human Genetics, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Innsbruck A-6020, Austria.
  • Parker MJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
  • Zakaria Z; Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield, S10 2TH, UK.
  • Choy YS; Institute for Medical Research, Kuala Lumpur, Jalan Pahang 50588, Malaysia.
  • Wieczorek D; Prince Court Medical Centre, Kuala Lumpur 50450, Malaysia.
  • Innes AM; Institute of Human Genetics, University Clinic Essen, Duisburg-Essen University, Essen 45122, Germany.
  • Jun KR; Institute of Human Genetics, University Clinic, Heinrich-Heine University, Düsseldorf 40225, Germany.
  • Zinner S; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada T3B 6A8.
  • Prin F; Department of Laboratory Medicine, Haeundae Paik Hospital, Inje University, Haeundae-gu, Busan, Korea.
  • Lygate CA; Seattle Children's Hospital, Seattle, WA 98105, USA.
  • Pretorius P; The Francis Crick Institute Mill Hill Laboratory, London NW7 1AA, UK.
  • Rosenfeld JA; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7BN, UK.
  • Mohun TJ; Department of Neuroradiology, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford OX3 9DU, UK.
  • Lu X; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cell Death Differ ; 23(12): 1973-1984, 2016 12.
Article in En | MEDLINE | ID: mdl-27447114

Full text: 1 Database: MEDLINE Main subject: Chromosome Deletion / Tumor Suppressor Proteins / Apoptosis Regulatory Proteins Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Chromosome Deletion / Tumor Suppressor Proteins / Apoptosis Regulatory Proteins Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Year: 2016 Type: Article