Letter: Delayed drug-induced dystonias.

nork Simpson, M A
Argitaratua 1973

Letter: An easy death--an uneasy argument.

nork Simpson, M A
Argitaratua 1975

Future of British psychiatrists.

nork Simpson, M A
Argitaratua 1971

Overseas students.

nork Simpson, M. A.
Argitaratua 1967

Living with the dying.

nork Simpson, M. A.
Argitaratua 1977

Female genital self-mutilation as a cause of vaginal bleeding

nork Simpson, M. A., Anstee, B. H.
Argitaratua 1974

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

nork Simpson, M A, Squires, T J, Busuttil, A
Argitaratua 2000

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

nork Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Argitaratua izan da Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

nork 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
Argitaratua izan da Mol Psychiatry (2018)

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

nork 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.
Argitaratua izan da J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

nork 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
Argitaratua 2014

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

nork 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
Argitaratua izan da Mol Psychiatry (2016)

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

nork 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
Argitaratua izan da Mol Psychiatry (2015)

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

nork 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. 
Argitaratua 2007