| Bibliographic Citation
| - ChevarinMartin, Duffourdyannis, a BarnardRebecca, MouttonSébastien, LecoquierreFrançois, DaoudFatma, KuentzPaul, CabretCaroline, ThevenonJulien, GautierElodie, CallierPatrick, St-OngeJudith, JouanThibaud, LacombeDidier, DelrueMarie Ange, GoizetCyril, Morice-PicardFanny, Van-GilsJulien, MunnichArnold, LyonnetStanislas, Cormier-DaireValérie, BaujatGeneviève, HolderMuriel, PetitFlorence, LeheupBruno, OdentSylvie, JoukPierre-Simon, LopezGipsy, GenevièveDavid, CollignonPatrick, Martin-CoignardDominique, JacquetteAurélia, PerrinLaurence, PutouxAudrey, SarrazinElisabeth, AmarofKhadija, MissotteIsabelle, CoubesChristine, JagadeeshSujatha, LapiElisabetta, DemurgerFlorence, GoldenbergAlice, Doco-FenzyMartine, MignotCyril, HéronDelphine, Jean-MarçaisNolwenn, MasurelAlice, El ChehadehSalima, MarleNathalie, HuetFrédéric, BinquetChristine, Collod-BeroudGwenaëlle, ArnaudPauline, HannaNadine, BoileauCatherine, JondeauGuillaume, OlasoRobert, LechnerDoris, PoeCharlotte, AssoumMirna, CarmignacVirginie, DuplombLaurence, Tran Mau-ThemFrédéric, PhilippeChristophe, VitobelloAntonio, BruelAnge-Line, BolandAnne, DeleuzeJean-François, Thauvin-RobinetChristel, RivièreJean-Baptiste, O'RoakBrian. Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability. Journal of Medical Genetics, BMJ Publishing Group, 2020, 57 (7), pp.466-474. ⟨10.1136/jmedgenet-2019-106425⟩
- ChevarinMartin, DuffourdYannis, a BarnardRebecca, MouttonSébastien, LecoquierreFrançois, DaoudFatma, KuentzPaul, CabretCaroline, ThevenonJulien, GautierElodie, CallierPatrick, St-OngeJudith, JouanThibaud, LacombeDidier, DelrueMarie Ange, GoizetCyril, Morice-PicardFanny, Van-GilsJulien, MunnichArnold, LyonnetStanislas, Cormier-DaireValérie, BaujatGeneviève, HolderMuriel, PetitFlorence, LeheupBruno, OdentSylvie, JoukPierre-Simon, LopezGipsy, GenevièveDavid, CollignonPatrick, Martin-CoignardDominique, JacquetteAurélia, PerrinLaurence, PutouxAudrey, SarrazinElisabeth, AmarofKhadija, MissotteIsabelle, CoubesChristine, JagadeeshSujatha, LapiElisabetta, DemurgerFlorence, GoldenbergAlice, Doco-FenzyMartine, MignotCyril, HéronDelphine, Jean-MarçaisNolwenn, MasurelAlice, El ChehadehSalima, MarleNathalie, HuetFrédéric, BinquetChristine, Collod-BeroudGwenaëlle, ArnaudPauline, HannaNadine, BoileauCatherine, JondeauGuillaume, OlasoRobert, LechnerDoris, PoeCharlotte, AssoumMirna, CarmignacVirginie, DuplombLaurence, Tran Mau-ThemFrédéric, PhilippeChristophe, VitobelloAntonio, BruelAnge-Line, BolandAnne, DeleuzeJean-François, Thauvin-RobinetChristel, RivièreJean-Baptiste, O'RoakBrian . Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability . Journal of Medical Genetics, 2020, 57 (7), pp.466-474 . ⟨10.1136/jmedgenet-2019-106425⟩
- Chevarin Martin, Duffourd Yannis, a Barnard Rebecca, Moutton Sébastien, Lecoquierre François, Daoud Fatma, Kuentz Paul, Cabret Caroline, Thevenon Julien, Gautier Elodie, Callier Patrick, St-Onge Judith, Jouan Thibaud, Lacombe Didier, Delrue Marie Ange, Goizet Cyril, Morice-Picard Fanny, Van-Gils Julien, Munnich Arnold, Lyonnet Stanislas, Cormier-Daire Valérie, Baujat Geneviève, Holder Muriel, Petit Florence, Leheup Bruno, Odent Sylvie, Jouk Pierre-Simon, Lopez Gipsy, Geneviève David, Collignon Patrick, Martin-Coignard Dominique, Jacquette Aurélia, Perrin Laurence, Putoux Audrey, Sarrazin Elisabeth, Amarof Khadija, Missotte Isabelle, Coubes Christine, Jagadeesh Sujatha, Lapi Elisabetta, Demurger Florence, Goldenberg Alice, Doco-Fenzy Martine, Mignot Cyril, Héron Delphine, Jean-Marçais Nolwenn, Masurel Alice, El Chehadeh Salima, Marle Nathalie, Huet Frédéric, Binquet Christine, Collod-Beroud Gwenaëlle, Arnaud Pauline, Hanna Nadine, Boileau Catherine, Jondeau Guillaume, Olaso Robert, Lechner Doris, Poe Charlotte, Assoum Mirna, Carmignac Virginie, Duplomb Laurence, Tran Mau-Them Frédéric, Philippe Christophe, Vitobello Antonio, Bruel Ange-Line, Boland Anne, Deleuze Jean-François, Thauvin-Robinet Christel, Rivière Jean-Baptiste, O'Roak Brian . Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability . Journal of Medical Genetics, 2020, 57 (7), pp.466-474 . ⟨10.1136/jmedgenet-2019-106425⟩
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