학술논문

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(예 : 2010-2015)
'학술논문' 에서 검색결과 3건 | 목록 1~10
Academic Journal
Stephenson, Sarah E. M.Costain, GregoryBlok, Laura E. R.Silk, Michael A.Nguyen, Thanh BinhDong, XiaominAlhuzaimi, Dana E.Dowling, James J.Walker, SusanAmburgey, KimberlyHayeems, Robin Z.Rodan, Lance H.Schwartz, Marc A.Picker, JonathanLynch, Sally A.Gupta, AditiRasmussen, Kristen J.Schimmenti, Lisa A.Klee, Eric W.Niu, ZhiyvAgre, Katherine E.Chilton, IlanaChung, Wendy K.Revah-Politi, AnyaAu, P. Y. BillieGriffith, ChristopherRacobaldo, MelissaRaas-Rothschild, AnnickBen Zeev, BruriaBarel, OrtalMoutton, SebastienMorice-Picard, FannyCarmignac, VirginieCornaton, JennyMarle, NathalieDevinsky, OrrinStimach, ChandlerWechsler, Stephanie BurnsHainline, Bryan E.Sapp, KatieWillems, MarjolaineBruel, AngelineDias, Kerith-RaeEvans, Carey-AnneRoscioli, TonySachdev, RaniTemple, Suzanna E. L.Zhu, YingBaker, Joshua J.Scheffer, Ingrid E.Gardiner, Fiona J.Schneider, Amy L.Muir, Alison M.Mefford, Heather C.Crunk, AmyHeise, Elizabeth M.Millan, FranciscaMonaghan, Kristin G.Person, RichardRhodes, LindsayRichards, SarahWentzensen, Ingrid M.Cogne, BenjaminIsidor, BertrandNizon, MathildeVincent, MarieBesnard, ThomasPiton, AmelieMarcelis, CarloKato, KohjiKoyama, NorihisaOgi, TomooGoh, Elaine Suk-YingRichmond, ChristopherAmor, David J.Boyce, Jessica O.Morgan, Angela T.Hildebrand, Michael S.Kaspi, AntonyBahlo, MelanieFridriksdottir, RunKatrinardottir, HildigunnurSulem, PatrickStefansson, KariBjornsson, Hans TomasMandelstam, SimoneMorleo, ManuelaMariani, MilenaScala, MarcelloAccogli, AndreaTorella, AnnalauraCapra, ValeriaWallis, MathewJansen, SandraWaisfisz, Quintende Haan, HugolineSadedin, SimonLim, Sze ChernWhite, Susan M.Ascher, David B.Schenck, AnnetteLockhart, Paul J.Christodoulou, JohnTan, Tiong YangTUDP Study GrpBroad Ctr Mendelian Genomics
AMERICAN JOURNAL OF HUMAN GENETICS; APR 7 2022, 109 4, p601-p617, 18p.
Electronic Resource
Küry , S , Ebstein , F , Undiagnosed Diseases Network , Mollé , A , Besnard , T , Lee , M K , Vignard , V , Hery , T , Nizon , M , Mancini , G M S , Giltay , J C , Cogné , B , McWalter , K , Deb , W , Mor-Shaked , H , Li , H , Schnur , R E , Wentzensen , I M , Denommé-Pichon , A S , Fourgeux , C , Verheijen , F W , Faurie , E , Schot , R , Stevens , C A , Smits , D J , Barr , E , Sheffer , R , Bernstein , J A , Stimach , C L , Kovitch , E , Shashi , V , Schoch , K , Smith , W , van Jaarsveld , R H , Hurst , A C E , Smith , K , Baugh , E H , Bohm , S G , Vyhnálková , E , Ryba , L , Delnatte , C , Neira , J , Bonneau , D , Toutain , A , Rosenfeld , J A , Audebert-Bellanger , S , Gilbert-Dussardier , B , Odent , S , Laumonnier , F , Berger , S I & Smith , A C M 2022 , ' Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder ' , American Journal of Human Genetics , vol. 109 , no. 2 , pp. 361-372 .
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[검색어] Stimach, Chandler L.
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