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1 Ergebnisse
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MYT1L-associated neurodevelopmental disorder: description o..:
Coursimault, Juliette
;
Guerrot, Anne-Marie
;
Morrow, Michelle
...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00439-021-02383-z. , 2022
Link:
https://hal.science/hal-03820933
RT Journal T1
MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects
UL https://suche.suub.uni-bremen.de/peid=base-ftunigrenoble:oai:HAL:hal-03820933v1&Exemplar=1&LAN=DE A1 Coursimault, Juliette A1 Guerrot, Anne-Marie A1 Morrow, Michelle A1 Schramm, Catherine A1 Zamora, Francisca Millan A1 Shanmugham, Anita A1 Liu, Shuxi A1 Zou, Fanggeng A1 Bilan, Frédéric A1 Le Guyader, Gwenaël A1 Bruel, Ange-Line A1 Denommé-Pichon, Anne-Sophie A1 Faivre, Laurence A1 Tran Mau-Them, Frédéric A1 Tessarech, Marine A1 Colin, Estelle A1 El Chehadeh, Salima A1 Gérard, Bénédicte A1 Schaefer, Elise A1 Cogne, Benjamin A1 Isidor, Bertrand A1 Nizon, Mathilde A1 Doummar, Diane A1 Valence, Stéphanie A1 Héron, Delphine A1 Keren, Boris A1 Mignot, Cyril A1 Coutton, Charles A1 Devillard, Françoise A1 Alaix, Anne-Sophie A1 Amiel, Jeanne A1 Colleaux, Laurence A1 Munnich, Arnold A1 Poirier, Karine A1 Rio, Marlène A1 Rondeau, Sophie A1 Barcia, Giulia A1 Callewaert, Bert A1 Dheedene, Annelies A1 Kumps, Candy A1 Vergult, Sarah A1 Menten, Björn A1 Chung, Wendy A1 Hernan, Rebecca A1 Larson, Austin A1 Nori, Kelly A1 Stewart, Sarah A1 Wheless, James A1 Kresge, Christina A1 Pletcher, Beth A1 Caumes, Roseline A1 Smol, Thomas A1 Sigaudy, Sabine A1 Coubes, Christine A1 Helm, Margaret A1 Smith, Rosemarie A1 Morrison, Jennifer A1 Wheeler, Patricia A1 Kritzer, Amy A1 Jouret, Guillaume A1 Afenjar, Alexandra A1 Deleuze, Jean-François A1 Olaso, Robert A1 Boland, Anne A1 Poitou, Christine A1 Frebourg, Thierry A1 Houdayer, Claude A1 Saugier-Veber, Pascale A1 Nicolas, Gaël A1 Lecoquierre, François PB HAL CCSD; Springer Verlag YR 2022 K1 MESH: Adolescent K1 MESH: Adult K1 MESH: Obesity K1 MESH: Phenotype K1 MESH: Transcription Factors K1 MESH: Young Adult K1 MESH: Child K1 Preschool K1 MESH: Epilepsy K1 MESH: Feeding and Eating Disorders K1 MESH: Female K1 MESH: Genetic Association Studies K1 MESH: Genetic Variation K1 MESH: Heterozygote K1 MESH: Humans K1 MESH: Infant K1 MESH: Language Development Disorders K1 MESH: Male K1 MESH: Nerve Tissue Proteins K1 MESH: Neurodevelopmental Disorders K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1007/s00439-021-02383-z LK http://dx.doi.org/https://hal.science/hal-03820933 DO https://hal.science/hal-03820933 SF ELIB - SuUB Bremen
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