检索结果 - Simpson, Michael A

Applying for Junior Hospital Posts 由 Simpson, Michael A.

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Delayed Drug-induced Dystonias 由 Simpson, Michael A.

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Fear of ECT 由 Simpson, Michael A

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Registration and the G.M.C 由 Simpson, Michael A.

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Intelligence and Fertility 由 Simpson, Michael A.

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Surgeons and Technical Skill 由 Simpson, Michael A.

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Living with the dying 由 Simpson, Michael A.

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Student Research 由 Simpson, Michael A.

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The Future of Genomics for Developmentalists 由 Plomin, Robert, Simpson, Michael A.

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Psoriasis and Genetics 由 DAND, Nick, MAHIL, Satveer K., CAPON, Francesca, SMITH, Catherine H., SIMPSON, Michael A., BARKER, Jonathan N.

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Network‐Informed Gene Ranking Tackles Genetic Heterogeneity in Exome‐Sequencing Studies of Monogenic Disease 由 Dand, Nick, Schulz, Reiner, Weale, Michael E., Southgate, Laura, Oakey, Rebecca J., Simpson, Michael A., Schlitt, Thomas

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Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia 由 Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.

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MED12, TERT promoter and RBM15 mutations in primary and recurrent phyllodes tumours 由 Garcia-Dios, Diego A, Levi, Dina, Shah, Vandna, Gillett, Cheryl, Simpson, Michael A, Hanby, Andrew, Tomlinson, Ian, Sawyer, Elinor J

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Mutation in GNE is associated with severe congenital thrombocytopenia 由 Futterer, Jane, Dalby, Amanda, Lowe, Gillian C., Johnson, Ben, Simpson, Michael A., Motwani, Jayashree, Williams, Mike, Watson, Steve P., Morgan, Neil V.

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Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome 由 Gray, Mary J, Kim, Chong Ae, Bertola, Debora Romeo, Arantes, Paula Ricci, Stewart, Helen, Simpson, Michael A, Irving, Melita D, Robertson, Stephen P

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Thinking positively: The genetics of high intelligence 由 Shakeshaft, Nicholas G., Trzaskowski, Maciej, McMillan, Andrew, Krapohl, Eva, Simpson, Michael A., Reichenberg, Avi, Cederlöf, Martin, Larsson, Henrik, Lichtenstein, Paul, Plomin, Robert

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A Three-Stage Genome-Wide Association Study of General Cognitive Ability: Hunting the Small Effects 由 Davis, Oliver S. P., Butcher, Lee M., Docherty, Sophia J., Meaburn, Emma L., Curtis, Charles J. C., Simpson, Michael A., Schalkwyk, Leonard C., Plomin, Robert

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Fine mapping genetic associations between the HLA region and extremely high intelligence 由 Zabaneh, Delilah, Krapohl, Eva, Simpson, Michael A., Miller, Mike B., Iacono, William G., McGue, Matt, Putallaz, Martha, Lubinski, David, Plomin, Robert, Breen, Gerome

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EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features 由 Ganetzky, Rebecca, Finn, Erin, Bagchi, Atrish, Zollo, Ornella, Conlin, Laura, Deardorff, Matthew, Harr, Margaret, Simpson, Michael A, McGrath, John A, Zackai, Elaine, Lemmon, Mark A, Sondheimer, Neal

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Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years 由 Petridis, Christos, Arora, Iteeka, Shah, Vandna, Megalios, Anargyros, Moss, Charlotte, Mera, Anca, Clifford, Angela, Gillett, Cheryl, Pinder, Sarah E., Tomlinson, Ian, Roylance, Rebecca, Simpson, Michael A., Sawyer, Elinor J.

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