Arama Sonuçları - Simpson, Michael A
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 81
- Sonraki Sayfaya Git
-
1
Applying for Junior Hospital Posts Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1973Metin -
2
Delayed Drug-induced Dystonias Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1974Metin -
3
-
4
Registration and the G.M.C Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1972Metin -
5
Intelligence and Fertility Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1972Metin -
6
Surgeons and Technical Skill Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1971Metin -
7
Living with the dying Yazar: Simpson, Michael A.
Baskı/Yayın Bilgisi 1978Metin -
8
-
9
The Future of Genomics for Developmentalists Yazar: Plomin, Robert, Simpson, Michael A.
Baskı/Yayın Bilgisi 2013Metin -
10
Psoriasis and Genetics Yazar: DAND, Nick, MAHIL, Satveer K., CAPON, Francesca, SMITH, Catherine H., SIMPSON, Michael A., BARKER, Jonathan N.
Baskı/Yayın Bilgisi 2020Metin -
11
Network‐Informed Gene Ranking Tackles Genetic Heterogeneity in Exome‐Sequencing Studies of Monogenic Disease Yazar: Dand, Nick, Schulz, Reiner, Weale, Michael E., Southgate, Laura, Oakey, Rebecca J., Simpson, Michael A., Schlitt, Thomas
Baskı/Yayın Bilgisi 2015Metin -
12
Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia Yazar: Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.
Baskı/Yayın Bilgisi 2003Metin -
13
MED12, TERT promoter and RBM15 mutations in primary and recurrent phyllodes tumours Yazar: Garcia-Dios, Diego A, Levi, Dina, Shah, Vandna, Gillett, Cheryl, Simpson, Michael A, Hanby, Andrew, Tomlinson, Ian, Sawyer, Elinor J
Baskı/Yayın Bilgisi 2018Metin -
14
Mutation in GNE is associated with severe congenital thrombocytopenia Yazar: Futterer, Jane, Dalby, Amanda, Lowe, Gillian C., Johnson, Ben, Simpson, Michael A., Motwani, Jayashree, Williams, Mike, Watson, Steve P., Morgan, Neil V.
Baskı/Yayın Bilgisi 2018Metin -
15
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome Yazar: Gray, Mary J, Kim, Chong Ae, Bertola, Debora Romeo, Arantes, Paula Ricci, Stewart, Helen, Simpson, Michael A, Irving, Melita D, Robertson, Stephen P
Baskı/Yayın Bilgisi 2012Metin -
16
Thinking positively: The genetics of high intelligence Yazar: Shakeshaft, Nicholas G., Trzaskowski, Maciej, McMillan, Andrew, Krapohl, Eva, Simpson, Michael A., Reichenberg, Avi, Cederlöf, Martin, Larsson, Henrik, Lichtenstein, Paul, Plomin, Robert
Baskı/Yayın Bilgisi 2015Metin -
17
A Three-Stage Genome-Wide Association Study of General Cognitive Ability: Hunting the Small Effects Yazar: 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
Baskı/Yayın Bilgisi 2010Metin -
18
Fine mapping genetic associations between the HLA region and extremely high intelligence Yazar: Zabaneh, Delilah, Krapohl, Eva, Simpson, Michael A., Miller, Mike B., Iacono, William G., McGue, Matt, Putallaz, Martha, Lubinski, David, Plomin, Robert, Breen, Gerome
Baskı/Yayın Bilgisi 2017Metin -
19
EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features Yazar: 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
Baskı/Yayın Bilgisi 2015Metin -
20
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 Yazar: 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.
Baskı/Yayın Bilgisi 2019Metin