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Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.
Bilo, Larissa; Ochoa, Eguzkine; Lee, Sunwoo; Dey, Daniela; Kurth, Ingo; Kraft, Florian; Rodger, Fay; Docquier, France; Toribio, Ana; Bottolo, Leonardo; Binder, Gerhard; Fekete, György; Elbracht, Miriam; Maher, Eamonn R; Begemann, Matthias; Eggermann, Thomas.
Affiliation
  • Bilo L; Medical Faculty, Institute for Human Genetics and Genome Medicine, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Ochoa E; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Lee S; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Dey D; Medical Faculty, Institute for Human Genetics and Genome Medicine, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Kurth I; Medical Faculty, Institute for Human Genetics and Genome Medicine, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Kraft F; Medical Faculty, Institute for Human Genetics and Genome Medicine, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Rodger F; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Docquier F; Stratified Medicine Core Laboratory NGS Hub, Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Toribio A; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Bottolo L; Stratified Medicine Core Laboratory NGS Hub, Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Binder G; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Fekete G; Stratified Medicine Core Laboratory NGS Hub, Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Elbracht M; Department of Medical Genetics, University of Cambridge, Cambridge, CB2 0QQ, UK.
  • Maher ER; MRC Biostatistics Unit, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Begemann M; The Alan Turing Institute, London, UK.
  • Eggermann T; Pediatric Endocrinology, University Children's Hospital, Universiy of Tuebingen, Tuebingen, Germany.
Clin Epigenetics ; 15(1): 35, 2023 03 01.
Article de En | MEDLINE | ID: mdl-36859312
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Méthylation de l'ADN / Génomique Type d'étude: Prognostic_studies / Risk_factors_studies Langue: En Journal: Clin Epigenetics Année: 2023 Type de document: Article Pays d'affiliation: Allemagne
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Méthylation de l'ADN / Génomique Type d'étude: Prognostic_studies / Risk_factors_studies Langue: En Journal: Clin Epigenetics Année: 2023 Type de document: Article Pays d'affiliation: Allemagne