Søgeresultater - Simpson, Michael A

Applying for Junior Hospital Posts af Simpson, Michael A.

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Delayed Drug-induced Dystonias af Simpson, Michael A.

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Fear of ECT af Simpson, Michael A

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

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Intelligence and Fertility af Simpson, Michael A.

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Surgeons and Technical Skill af Simpson, Michael A.

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Living with the dying af Simpson, Michael A.

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Student Research af Simpson, Michael A.

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

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Psoriasis and Genetics af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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 af 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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