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Castilla-Vallmanya, LauraSelmer, Kaja K.Dimartino, ClemantineRabionet, RaquelBlanco-Sanchez, BernardoYang, SandraReijnders, Margot R. F.van Essen, Antonie J.Oufadem, MyriamVigeland, Magnus D.Stadheim, BarbroHouge, GunnarCox, HelenKingston, HelenClayton-Smith, JillInnis, Jeffrey W.Iascone, MariaCereda, AnnaGabbiadini, SaraChung, Wendy K.Sanders, VictoriaCharrow, JoelBryant, EmilyMillichap, JohnVitobello, AntonioThauvin, ChristelMau-Them, Frederic TranFaivre, LaurenceLesca, GaetanLabalme, AudreyRougeot, ChristelleChatron, NicolasSanlaville, DamienChristensen, Katherine M.Kirby, AmeliaLewandowski, RaymondGannaway, RachelAly, MahaLehman, AnnaClarke, LorneGraul-Neumann, LuitgardZweier, ChristianeLessel, DavorLozic, BernardaAukrust, IngvildPeretz, RyanStratton, RobertSmol, ThomasDieux-Coeslier, AnneMeira, JoannaWohler, ElizabethSobreira, NaraBeaver, Erin M.Heeley, JenniferBriere, Lauren C.High, Frances A.Sweetser, David A.Walker, Melissa A.Keegan, Catherine E.Jayakar, ParulShinawi, MarwanKerstjens-Frederikse, Wilhelmina S.Earl, Dawn L.Siu, Victoria M.Reesor, EmmaYao, TonyHegele, Robert A.Vaske, Olena M.Rego, ShannonShapiro, Kevin A.Wong, BrianGambello, Michael J.McDonald, MarieKarlowicz, DanielleColombo, RobertoSerretti, AlessandroPais, LynnO'Donnell-Luria, AnneWray, AlisonSadedin, SimonChong, BelindaTan, Tiong Y.Christodoulou, JohnWhite, Susan M.Slavotinek, AnneBarbouth, DeborahSwols, Dayna MorelParisot, MelanieBole-Feysot, ChristineNitschke, PatrickPingault, VeroniqueMunnich, ArnoldCho, Megan T.Cormier-Daire, ValerieBalcells, SusannaLyonnet, StanislasGrinberg, DanielAmiel, JeanneUrreizti, RoserGordon, Christopher T.Undiagnosed Dis NetworkCare4Rare Canada Consortium
GENETICS IN MEDICINE; JUL 2020, 22 7, p1215-p1226, 12p.
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[AR] Blanco-Sánchez, Bernardo
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