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Further delineation of the MECP2 duplication syndrome pheno..:
Miguet, Marguerite
;
Faivre, Laurence
;
Amiel, Jeanne
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2017-104956. , 2018
Link:
https://u-bourgogne.hal.science/hal-02064139
RT Journal T1
Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features
UL https://suche.suub.uni-bremen.de/peid=base-ftsorbonneuniv:oai:HAL:hal-02064139v1&Exemplar=1&LAN=DE A1 Miguet, Marguerite A1 Faivre, Laurence A1 Amiel, Jeanne A1 Nizon, Mathilde A1 Touraine, Renaud A1 Prieur, Fabienne A1 Pasquier, Laurent A1 Lefebvre, Mathilde A1 Thevenon, Julien A1 Dubourg, Christèle A1 Julia, Sophie A1 Sarret, Catherine A1 Remerand, Ganaëlle A1 Francannet, Christine A1 Laffargue, Fanny A1 Boespflug-Tanguy, Odile A1 David, Albert A1 Isidor, Bertrand A1 Vigneron, Jacqueline A1 Leheup, Bruno A1 Lambert, Laetitia A1 Philippe, Christophe A1 Beri-Dexheimer, Mylène A1 Cuisset, Jean-Marie A1 Andrieux, Joris A1 Plessis, Ghislaine A1 Toutain, Annick A1 Guibaud, Laurent A1 Cormier-Daire, Valérie A1 Rio, Marlène A1 Bonnefont, Jean-Paul A1 Echenne, Bernard A1 Journel, Hubert A1 Burglen, Lydie A1 Chantot-Bastaraud, Sandrine A1 Bienvenu, Thierry A1 Baumann, Clarisse A1 Perrin, Laurence A1 Drunat, Séverine A1 Jouk, Pierre-Simon A1 Dieterich, Klaus A1 Devillard, Françoise A1 Lacombe, Didier A1 Philip, Nicole A1 Sigaudy, Sabine A1 Moncla, Anne A1 Missirian, Chantal A1 Badens, Catherine A1 Perreton, Nathalie A1 Thauvin-Robinet, Christel A1 Achro-Puce, Réseau A1 Pedespan, Jean-Michel A1 Rooryck, Caroline A1 Goizet, Cyril A1 Vincent-Delorme, Catherine A1 Duban-Bedu, Bénédicte A1 Bahi-Buisson, Nadia A1 Afenjar, Alexandra A1 Maincent, Kim A1 Héron, Delphine A1 Alessandri, Jean-Luc A1 Martin-Coignard, Dominique A1 Lesca, Gaetan A1 Rossi, Massimiliano A1 Raynaud, Martine A1 Callier, Patrick A1 Mosca-Boidron, Anne-Laure A1 Marle, Nathalie A1 Coutton, Charles A1 Satre, Véronique A1 Caignec, Cédric Le A1 Malan, Valérie A1 Romana, Serge A1 Keren, Boris A1 Tabet, Anne-Claude A1 Kremer, Valérie A1 Scheidecker, Sophie A1 Vigouroux, Adeline A1 Lackmy-Port-Lis, Marilyn A1 Sanlaville, Damien A1 Till, Marianne A1 Carneiro, Maryline A1 Gilbert-Dussardier, Brigitte A1 Willems, Marjolaine A1 van Esch, Hilde A1 Portes, Vincent Des A1 El Chehadeh, Salima PB HAL CCSD; BMJ Publishing Group YR 2018 K1 MECP2gene K1 X-linked K1 Xq28 duplication K1 facial dysmorphism K1 genetic counselling K1 MECP2duplication syndrome K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2017-104956 LK http://dx.doi.org/https://u-bourgogne.hal.science/hal-02064139 DO https://u-bourgogne.hal.science/hal-02064139 SF ELIB - SuUB Bremen
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