Canlyniadau Chwilio - Simpson, M A

Letter: Delayed drug-induced dystonias. gan Simpson, M A

Cael y testun llawn Cael y testun llawn

Letter: An easy death--an uneasy argument. gan Simpson, M A

Cael y testun llawn Cael y testun llawn

Future of British psychiatrists. gan Simpson, M A

Cael y testun llawn Cael y testun llawn

Overseas students. gan Simpson, M. A.

Cael y testun llawn Cael y testun llawn

Living with the dying. gan Simpson, M. A.

Cael y testun llawn Cael y testun llawn

Female genital self-mutilation as a cause of vaginal bleeding gan Simpson, M. A., Anstee, B. H.

Cael y testun llawn

The case of Jane Anderson, Portobello, 1889-1914. gan Simpson, M A, Squires, T J, Busuttil, A

Cael y testun llawn Cael y testun llawn

New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy gan Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis gan Walsh, D. M., Shah, S. H., Simpson, M. A., Morgan, N. V., Khaliq, S., Trembath, R. C., Mehdi, S. Q., Maher, E. R.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

A genome-wide association study for extremely high intelligence gan Zabaneh, D, Krapohl, E, Gaspar, H A, Curtis, C, Lee, S H, Patel, H, Newhouse, S, Wu, H M, Simpson, M A, Putallaz, M, Lubinski, D, Plomin, R, Breen, G

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders gan Leo, V. C., Morgan, N. V., Bem, D., Jones, M. L., Lowe, G. C., Lordkipanidzé, M., Drake, S., Simpson, M. A., Gissen, P., Mumford, A., Watson, S. P., Daly, M. E.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Germline CDH1 mutations in bilateral lobular carcinoma in situ gan Petridis, C, Shinomiya, I, Kohut, K, Gorman, P, Caneppele, M, Shah, V, Troy, M, Pinder, S E, Hanby, A, Tomlinson, I, Trembath, R C, Roylance, R, Simpson, M A, Sawyer, E J

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence gan Spain, S L, Pedroso, I, Kadeva, N, Miller, M B, Iacono, W G, McGue, M, Stergiakouli, E, Smith, G D, Putallaz, M, Lubinski, D, Meaburn, E L, Plomin, R, Simpson, M A

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development gan Simpson, M. A. , Hsu, R. , Keir, L. S. , Hao, J. , Sivapalan, G. , Ernst, L. M. , Zackai, E. H. , Al-Gazali, L. I. , Hulskamp, G. , Kingston, H. M. , Prescott, T. E. , Ion, A. , Patton, M. A. , Murday, V. , George, A. , Crosby, A. H. 

Cael y testun llawn Cael y testun llawn