Letter: Delayed drug-induced dystonias.

Autor Simpson, M A
Vydáno 1973

Letter: An easy death--an uneasy argument.

Autor Simpson, M A
Vydáno 1975

Future of British psychiatrists.

Autor Simpson, M A
Vydáno 1971

Overseas students.

Autor Simpson, M. A.
Vydáno 1967

Living with the dying.

Autor Simpson, M. A.
Vydáno 1977

Female genital self-mutilation as a cause of vaginal bleeding

Autor Simpson, M. A., Anstee, B. H.
Vydáno 1974

The case of Jane Anderson, Portobello, 1889-1914.

Autor Simpson, M A, Squires, T J, Busuttil, A
Vydáno 2000

New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy

Autor Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Vydáno v Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

Autor Walsh, D. M., Shah, S. H., Simpson, M. A., Morgan, N. V., Khaliq, S., Trembath, R. C., Mehdi, S. Q., Maher, E. R.
Vydáno 2012

A genome-wide association study for extremely high intelligence

Autor 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
Vydáno v Mol Psychiatry (2018)

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

Autor 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.
Vydáno v J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

Autor 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
Vydáno 2014

A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

Autor 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
Vydáno v Mol Psychiatry (2016)

Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

Autor 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
Vydáno v Mol Psychiatry (2015)

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development

Autor 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. 
Vydáno 2007