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Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Bens, Susanne; Kolarova, Julia; Beygo, Jasmin; Buiting, Karin; Caliebe, Almuth; Eggermann, Thomas; Gillessen-Kaesbach, Gabriele; Prawitt, Dirk; Thiele-Schmitz, Susanne; Begemann, Matthias; Enklaar, Thorsten; Gutwein, Jana; Haake, Andrea; Paul, Ulrike; Richter, Julia; Soellner, Lukas; Vater, Inga; Monk, David; Horsthemke, Bernhard; Ammerpohl, Ole; Siebert, Reiner.
Affiliation
  • Bens S; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Kolarova J; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Beygo J; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, D 45122 Essen, Germany.
  • Buiting K; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, D 45122 Essen, Germany.
  • Caliebe A; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Eggermann T; Institute of Human Genetics, University Hospital Aachen, D 52074 Aachen, Germany.
  • Gillessen-Kaesbach G; Institut für Humangenetik Lübeck, Universität zu Lübeck, D 23562 Lübeck, Germany.
  • Prawitt D; Section of Molecular Pediatrics University Medical Centre of the Johannes Gutenberg-University Mainz, D 55131 Mainz, Germany.
  • Thiele-Schmitz S; Division of Experimental Paediatric Endocrinology & Diabetes, Department of Paediatrics, University of Lübeck, D 23562 Lübeck, Germany.
  • Begemann M; Institute of Human Genetics, University Hospital Aachen, D 52074 Aachen, Germany.
  • Enklaar T; Section of Molecular Pediatrics University Medical Centre of the Johannes Gutenberg-University Mainz, D 55131 Mainz, Germany.
  • Gutwein J; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Haake A; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Paul U; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Richter J; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Soellner L; Institute of Human Genetics, University Hospital Aachen, D 52074 Aachen, Germany.
  • Vater I; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Monk D; Institut d'Investigació Biomedica de Bellvitge (IDIBELL), Cancer Epigenetic & Biology Program (PEBC), Catalan Institute of Oncology, Hospital Duran i Reynals Barcelona, Barcelona, ES 08907, Spain.
  • Horsthemke B; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, D 45122 Essen, Germany.
  • Ammerpohl O; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
  • Siebert R; Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, D 24105 Kiel, Germany.
Epigenomics ; 8(6): 801-16, 2016 06.
Article in En | MEDLINE | ID: mdl-27323310
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Genomic Imprinting / DNA Methylation Type of study: Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Epigenomics Year: 2016 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Genomic Imprinting / DNA Methylation Type of study: Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Epigenomics Year: 2016 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido