海量图书期刊资源,随时随地畅享阅读乐趣
An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.Barnes, I C; Curtis, D J; Duncan, S L · Journal of Medical Genetics · 1987
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathwaysO'Dushlaine, Colm; Rossin, Lizzy; Lee, Phil H; Duncan, Laramie; Parikshak, Neelroop N; Newhouse, Stephen; Ripke, Stephan; Neale, Benjamin M; Purcell, Shaun M; Posthuma, Danielle; Nurnberger, John I; Lee, S Hong; Faraone, Stephen V; Perlis, Roy H; Mowry, Bryan J; Thapar, Anita; Goddard, Michael E; Witte, John S; Absher, Devin; Agartz, Ingrid; Akil, Huda; Amin, Farooq; Andreassen, Ole A; Anjorin, Adebayo; Anney, Richard; Anttila, Verneri; Arking, Dan E; Asherson, Philip; Azevedo, Maria H; Backlund, Lena; Badner, Judith A; Bailey, Anthony J; Banaschewski, Tobias; Barchas, Jack D; Barnes, Michael R; Barrett, Thomas B; Bass, Nicholas; Battaglia, Agatino; Bauer, Michael; Bayés, Mònica; Bellivier, Frank; Bergen, Sarah E; Berrettini, Wade; Betancur, Catalina; Bettecken, Thomas; Biederman, Joseph; Binder, Elisabeth B; Black, Donald W; Blackwood, Douglas H R; Bloss, Cinnamon S; Boehnke, Michael; Boomsma, Dorret I; Breuer, René; Bruggeman, Richard; Cormican, Paul; Buccola, Nancy G; Buitelaar, Jan K; Bunney, William E; Buxbaum, Joseph D; Byerley, William F; Byrne, Enda M; Caesar, Sian; Cahn, Wiepke; Cantor, Rita M; Casas, Miguel; Chakravarti, Aravinda; Chambert, Kimberly; Choudhury, Khalid; Cichon, Sven; Mattheisen, Manuel; Cloninger, C Robert; Collier, David A; Cook, Edwin H; Coon, Hilary; Cormand, Bru; Corvin, Aiden; Coryell, William H; Craig, David W; Craig, Ian W; Crosbie, Jennifer; Cuccaro, Michael L; Curtis, David; Czamara, Darina; Datta, Susmita; Dawson, Geraldine; Day, Richard; De Geus, Eco J; Degenhardt, Franziska; Djurovic, Srdjan; Donohoe, Gary J; Doyle, Alysa E; Duan, Jubao; Dudbridge, Frank; Duketis, Eftichia; Ebstein, Richard P; Edenberg, Howard J; Elia, Josephine; Ennis, Sean; Etain, Bruno; Fanous, Ayman; Farmer, Anne E; Ferrier, I Nicol; Flickinger, Matthew; Fombonne, Eric; Foroud, Tatiana; Frank, Josef; Franke, Barbara; Fraser, Christine; Freedman, Robert; Freimer, Nelson B; Freitag, Christine M; Friedl, Marion; Frisén, Louise; Gallagher, Louise; Gejman, Pablo · Nature Neuroscience · 2015
Barth syndromeJefferies, John L. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2013
Congenital microcephalyAlcantara, Diana; O'Driscoll, Mark · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Introduction: Brain malformationsMirzaa, Ghayda M.; Paciorkowski, Alex R. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Pontocerebellar hypoplasiaRudnik-Schöneborn, Sabine; Barth, Peter G.; Zerres, Klaus · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Pallister-Killian syndromeIzumi, Kosuke; Krantz, Ian D. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Cytogenetic highlights and transitionsSpinner, Nancy B. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016
IntroductionAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016
Publication schedule for 2016American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016