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Kaiser, Frank J.Ansari, MoradBraunholz, DianaGil-Rodríguez, María ConcepciónDecroos, ChristopheWilde, Jonathan J.Fincher, Christopher T.Kaur, ManinderBando, MasashigeAmor, David J.Atwal, Paldeep S.Bahlo, MelanieBowman, Christine M.Bradley, Jacquelyn J.Brunner, Han G.Clark, DinahDel Campo, MiguelDi Donato, NataliyaDiakumis, PeterDubbs, HollyDyment, David A.Eckhold, JulianeErnst, SarahFerreira, Jose C.Francey, Lauren J.Gehlken, UlrikeGuillén-Navarro, EncarnaGyftodimou, YolandaHall, Bryan D.Hennekam, RaoulHudgins, LouanneHullings, MelanieHunter, Jennifer M.Yntema, HelgerInnes, Micheil A.Kline, Antonie D.Krumina, ZitaLee, HaneLeppig, KathleenLynch, Sally AnnMallozzi, Mark B.Mannini, LindaMckee, ShaneMehta, Sarju G.Micule, IevaMohammed, ShehlaMoran, EllenMortier, Geert R.Moser, Joe-Ann S.Noon, Sarah E.Nozaki, NaohitoNunes, LuisPappas, John G.Penney, Lynette S.Pérez-Aytés, AntonioPetersen, Michael B.Puisac, BeatrizRevencu, NicoleRoeder, ElizabethSaitta, SulagnaScheuerle, Angela E.Schindeler, Karen L.Siu, Victoria M.Stark, ZornitzaStrom, Samuel P.Thiese, HeidiVater, IngaWillems, PatrickWilliamson, KathleenWilson, Louise C.Hakonarson, HakonQuintero-Rivera, FabiolaWierzba, JolantaMusio, AntonioGillessen-Kaesbach, GabrieleRamos, Feliciano J.Jackson, Laird G.Shirahige, KatsuhikoPié, JuanChristianson, David W.Krantz, Ian D.Fitzpatrick, David R.Deardorff, Matthew A.
Human Molecular Genetics. Jun 01, 2014 23(11):2888-2900
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UCL - SSS/IREC - Institut de recherche expérimentale et cliniqueUCL - (SLuc) Centre de génétique médicale UCLUCL - (SLuc) Centre de malformations vasculaires congénitalesKaiser, Frank J.Ansari, MoradBraunholz, DianaGil-Rodríguez, María ConcepciónDecroos, ChristopheWilde, Jonathan J.Fincher, Christopher T.Kaur, ManinderBando, MasashigeAmor, David J.Atwal, P.S.Bahlo, MelanieBowman, Christine M.Bradley, Jacquelyn J.Brunner, Han G.Clark, DinahCampo, Miguel DelDi Donato, NataliyaDiakumis, PeterDubbs, HollyDyment, David A.Eckhold, JulianeErnst, SarahFerreira, Jose C.Francey, Lauren J.Gehlken, UlrikeGuillén-Navarro, EncarnaGyftodimou, YolandaHall, Bryan D.Hennekam, RaoulHudgins, LouanneHullings, MelanieHunter, Jennifer M.Yntema, HelgerInnes, A. MicheilKline, Antonie D.Krumina, ZitaLee, HaneLeppig, KathleenLynch, Sally AnnMallozzi, Mark B.Mannini, LindaMckee, ShaneMehta, Sarju G.Micule, IevaConsortium, Care Rare CanadaMohammed, ShehlaMoran, EllenMortier, Geert R.Moser, Joe-Ann S.Noon, Sarah E.Nozaki, NaohitoNunes, LuisPappas, John G.Penney, Lynette S.Pérez-Aytés, AntonioPetersen, Michael B.Puisac, BeatrizRevencu, NicoleRoeder, ElizabethSaitta, SulagnaScheuerle, Angela E.Schindeler, Karen L.Siu, Victoria M.Stark, ZornitzaStrom, Samuel P.Thiese, HeidiVater, IngaWillems, P.Williamson, KathleenWilson, Louise C.Hakonarson, HakonQuintero-Rivera, FabiolaWierzba, JolantaMusio, AntonioGillessen-Kaesbach, GabrieleRamos, Feliciano J.Jackson, Laird G.Shirahige, KatsuhikoPié, JuanChristianson, David W.Krantz, Ian D.Fitzpatrick, David R.Deardorff, Matthew A.
Human Molecular Genetics, Vol. 23, no. 11, p. 2888-2900 (2014)
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[AR] Moser, Joe‐Ann S.
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