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O’Donnell-Luria, Anne HPais, Lynn SFaundes, VíctorWood, Jordan CSveden, AbigailLuria, VictorJamra, Rami AbouAccogli, AndreaAmburgey, KimberlyAnderlid, Britt MarieAzzarello-Burri, SilviaBasinger, Alice ABianchini, ClaudiaBird, Lynne MBuchert, RebeccaCarre, WilfridCeulemans, SophiaCharles, PerrineCox, HelenCulliton, LisaCurrò, AuroraStudy, Deciphering Developmental DisordersMcRae, Jeremy FClayton, StephenFitzgerald, Tomas WKaplanis, JoannaPrigmore, ElenaRajan, DianaSifrim, AlejandroAitken, StuartAkawi, NadiaAlvi, MohsanAmbridge, KirstyBarrett, Daniel MBayzetinova, TanyaJones, PhilipJones, Wendy DKing, DanielKrishnappa, NetravathiMason, Laura ESingh, TarjinderTivey, Adrian RAhmed, MunazaAnjum, UrujArcher, HayleyArmstrong, RuthAwada, JanaBalasubramanian, MeenaBanka, SiddharthBaralle, DianaBarnicoat, AngelaBatstone, PaulBaty, DavidBennett, ChrisBerg, JonathanBernhard, BirgittaBevan, A PaulBitner-Glindzicz, MariaBlair, EdwardBlyth, MoiraBohanna, DavidBourdon, LouiseBourn, DavidBradley, LisaBrady, AngelaBrent, SimonBrewer, CaroleBrunstrom, KateBunyan, David JBurn, JohnCanham, NatalieCastle, BruceChandler, KateChatzimichali, ElenaCilliers, DeirdreClarke, AngusClasper, SusanClayton-Smith, JillClowes, VirginiaCoates, AndreaCole, TrevorColgiu, IrinaCollins, AmandaCollinson, Morag NConnell, FionaCooper, NicolaCresswell, LaraCross, GarethCrow, YanickD’Alessandro, MariellaDabir, TabibDavidson, RosemarieDavies, Sallyde Vries, DylanDean, JohnDeshpande, CharuDevlin, GemmaDixit, AbhijitDobbie, Angus
American Journal of Human Genetics. 104(6)
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Küry, Sébastienvan Woerden, Geeske MBesnard, ThomasOnori, Martina ProiettiLatypova, XéniaTowne, Meghan CCho, Megan TPrescott, Trine EPloeg, Melissa ASanders, StephanStessman, Holly AFPujol, AuroraDistel, BenRobak, Laurie ABernstein, Jonathan ADenommé-Pichon, Anne-SophieLesca, GaëtanSellars, Elizabeth ABerg, JonathanCarré, WilfridBusk, Øyvind Løvoldvan Bon, Bregje WMWaugh, Jeff LDeardorff, MatthewHoganson, George EBosanko, Katherine BJohnson, Diana SDabir, TabibHolla, Øystein LundeSarkar, AjoyTveten, Kristiande Bellescize, JulittaBraathen, Geir JTerhal, Paulien AGrange, Dorothy Kvan Haeringen, ArieLam, ChristinaMirzaa, GhaydaBurton, JenniferBhoj, Elizabeth JDouglas, JessicaSantani, Avni BNesbitt, Addie IHelbig, Katherine LAndrews, Marisa VBegtrup, AmberTang, Shavan Gassen, Koen LIJuusola, JaneFoss, KimberlyEnns, Gregory MMoog, UteHinderhofer, KatrinParamasivam, NagarajanLincoln, SharynKusako, Brandon HLindenbaum, PierreCharpentier, EricNowak, Catherine BCherot, ElouanSimonet, ThomasRuivenkamp, Claudia ALHahn, SihounBrownstein, Catherine AXia, FanSchmitt, SébastienDeb, WallidBonneau, DominiqueNizon, MathildeQuinquis, DelphineChelly, JamelRudolf, GabrielleSanlaville, DamienParent, PhilippeGilbert-Dussardier, BrigitteToutain, AnnickSutton, Vernon RThies, JennyPeart-Vissers, Lisenka ELMBoisseau, PierreVincent, MarieGrabrucker, Andreas MDubourg, ChristèleNetwork, Undiagnosed DiseasesTan, Wen-HannVerbeek, Nienke EGranzow, MartinSanten, Gijs WEShendure, JayIsidor, BertrandPasquier, LaurentRedon, RichardYang, YapingState, Matthew WKleefstra, TjitskeCogné, BenjaminHUGO, GEMStudy, Deciphering Developmental DisordersPetrovski, SlavéRetterer, Kyle
American Journal of Human Genetics. 101(5)
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[AR] Carré, Wilfrid
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