학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 6건 | 목록 1~10
Academic Journal
Helbig, Katherine L.Lauerer, Robert J.Bahr, Jacqueline C.Souza, Ivana A.Myers, Candace T.Uysal, BetuelSchwarz, NiklasGandini, Maria A.Huang, SunKeren, BorisMignot, CyrilAfenjar, Alexandrade Villemeur, Thierry BilletteHeron, DelphineNava, CarolineValence, StephanieBuratti, JulienFagerberg, Christina R.Soerensen, Kristina P.Kibaek, MariaKamsteeg, Erik-JanKoolen, David A.Gunning, BoudewijnSchelhaas, H. JurgenKruer, Michael C.Fox, JordanaBakhtiari, SomayehJarrar, RandaPadilla-Lopez, SergioLindstrom, KristinJin, Sheng ChihZeng, XueBilguvar, KayaPapavasileiou, AntigoneXin, QingheZhu, ChanglianBoysen, KatjaVairo, FilippoLanpher, Brendan C.Klee, Eric W.Tillema, Jan-MendeltPayne, Eric T.Cousin, Margot A.Kruisselbrink, Teresa M.Wick, Myra J.Baker, JoshuaHaan, EricSmith, NicholasCorbett, Mark A.MacLennan, Alastair H.Gecz, JozefBiskup, SaskiaGoldmann, EvaRodan, Lance H.Kichula, ElizabethSegal, EricJackson, Kelly E.Asamoah, AlexanderDimmock, DavidMcCarrier, JulieBotto, Lorenzo D.Filloux, FrancisTvrdik, TatianaCascino, Gregory D.Klingerman, SherryNeumann, CatherineWang, RaymondJacobsen, Jessie C.Nolan, Melinda A.Snell, Russell G.Lehnert, KlausSadleir, Lynette G.Anderlid, Britt-MarieKvarnung, MalinGuerrini, RenzoFriez, Michael J.Lyons, Michael J.Leonhard, JenniferKringlen, GabrielCasas, KariEl Achkar, Christelle M.Smith, Lacey A.Rotenberg, AlexanderPoduri, AnnapurnaSanchis-Juan, AlbaCarss, Keren J.Rankin, JuliaZeman, AdamRaymond, F. LucyBlyth, MoiraKerr, BronwynRuiz, KarlaUrquhart, JillHughes, ImeldaBanka, SiddharthHedrich, Ulrike B. S.Scheffer, Ingrid E.Helbig, IngoZamponi, Gerald W.Lerche, HolgerMefford, Heather C.Deciphering Dev Disorders Study
AMERICAN JOURNAL OF HUMAN GENETICS; NOV 1 2018, 103 5, p666-p678, 13p.
Academic Journal
Oates, Emily C.Jones, Kristi J.Donkervoort, SandraCharlton, AmandaBrammah, SusanSmith, John E.Ware, James S.Yau, Kyle S.Swanson, Lindsay C.Whiffin, NicolaPeduto, Anthony J.Bournazos, AdamWaddell, Leigh B.Farrar, Michelle A.Sampaio, Hugo A.Teoh, Hooi LingLamont, Phillipa J.Mowat, DavidFitzsimons, Robin B.Corbett, Alastair J.Ryan, Monique M.O'Grady, Gina L.Sandaradura, Sarah A.Ghaoui, RoulaJoshi, HimanshuMarshall, Jamie L.Nolan, Melinda A.Kaur, SimranpreetPunetha, JayaToepf, AnaHarris, ElizabethBakshi, MadhuraGenetti, Casie A.Marttila, MinttuWerlauff, UllaStreichenberger, NathaliePestronk, AlanMazanti, IngridPinner, Jason R.Vuillerot, CaroleGrosmann, CarlaCamacho, AnaMohassel, PayamLeach, Meganne E.Foley, A. ReghanBharucha-Goebel, DianaCollins, JamesConnolly, Anne M.Gilbreath, Heather R.Iannaccone, Susan T.Castro, DianaCummings, Beryl B.Webster, Richard I.Lazaro, LeilaVissing, JohnCoppens, SandraDeconinck, NicolasLuk, Ho-MingThomas, Neil H.Foulds, Nicola C.Illingworth, Marjorie A.Ellard, SianMcLean, Catriona A.Phadke, RahulRavenscroft, GianinaWitting, NannaHackman, PeterRichard, IsabelleCooper, Sandra T.Kamsteeg, Erik-JanHoffman, Eric P.Bushby, KateStraub, VolkerUdd, BjarneFerreiro, AnaNorth, Kathryn N.Clarke, Nigel F.Lek, MonkolBeggs, Alan H.Boennemann, Carsten G.MacArthur, Daniel G.Granzier, HenkDavis, Mark R.Laing, Nigel G.
ANNALS OF NEUROLOGY; JUN 2018, 83 6, p1105-p1124, 20p.
Academic Journal
Helbig, Katherine L.Lauerer, Robert J.Bahr, Jacqueline C.Souza, Ivana A.Myers, Candace T.Uysal, BetulSchwarz, NiklasGandini, Maria A.Huang, SunKeren, BorisMignot, CyrilAfenjar, Alexandrade Villemeur, Thierry BilletteHeron, DelphineNava, CarolineValence, StephanieBuratti, JulienFagerberg, Christina R.Soerensen, Kristina P.Kibaek, MariaKamsteeg, Erik-JanKoolen, David A.Gunning, BoudewijnSchelhaas, H. JurgenKruer, Michael C.Fox, JordanaBakhtiari, SomayehJarrar, RandaPadilla-Lopez, SergioLindstrom, KristinJin, Sheng ChihZeng, XueBilguvar, KayaPapavasileiou, AntigoneXing, QingheZhu, ChanglianBoysen, KatjaVairo, FilippoLanpher, Brendan C.Klee, Eric W.Tillema, Jan-MendeltPayne, Eric T.Cousin, Margot A.Kruisselbrink, Teresa M.Wick, Myra J.Baker, JoshuaHaan, EricSmith, NicholasSadeghpour, AzitaDavis, Erica E.Katsanis, NicholasCorbett, Mark A.MacLennan, Alastair H.Gecz, JozefBiskup, SaskiaGoldmann, EvaRodan, Lance H.Kichula, ElizabethSegal, EricJackson, Kelly E.Asamoah, AlexanderDimmock, DavidMcCarrier, JulieBotto, Lorenzo D.Filloux, FrancisTvrdik, TatianaCascino, Gregory D.Klingerman, SherryNeumann, CatherineWang, RaymondJacobsen, Jessie C.Nolan, Melinda A.Snell, Russell G.Lehnert, KlausSadleir, Lynette G.Anderlid, Britt-MarieKvarnung, MalinGuerrini, RenzoFriez, Michael J.Lyons, Michael J.Leonhard, JenniferKringlen, GabrielCasas, KariEl Achkar, Christelle M.Smith, Lacey A.Rotenberg, AlexanderPoduri, AnnapurnaSanchis-Juan, AlbaCarss, Keren J.Rankin, JuliaZeman, AdamRaymond, F. LucyBlyth, MoiraKerr, BronwynRuiz, KarlaUrquhart, JillHughes, ImeldaBanka, SiddharthHedrich, Ulrike B. S.Scheffer, Ingrid E.Helbig, IngoZamponi, Gerald W.Lerche, HolgerMefford, Heather C.Task Force Neonatal GenomicsDeciphering Dev Disorders Study
AMERICAN JOURNAL OF HUMAN GENETICS; MAR 7 2019, 104 3, p562-p562, 1p.
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제한된 항목
[AR] Nolan, Melinda A.
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