Letter: Delayed drug-induced dystonias.

gan Simpson, M A
Cyhoeddwyd 1973

Letter: An easy death--an uneasy argument.

gan Simpson, M A
Cyhoeddwyd 1975

Future of British psychiatrists.

gan Simpson, M A
Cyhoeddwyd 1971

Overseas students.

gan Simpson, M. A.
Cyhoeddwyd 1967

Living with the dying.

gan Simpson, M. A.
Cyhoeddwyd 1977

Female genital self-mutilation as a cause of vaginal bleeding

gan Simpson, M. A., Anstee, B. H.
Cyhoeddwyd 1974

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

gan Simpson, M A, Squires, T J, Busuttil, A
Cyhoeddwyd 2000

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.
Cyhoeddwyd yn Am J Med Genet A (2016)

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.
Cyhoeddwyd 2012

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
Cyhoeddwyd yn Mol Psychiatry (2018)

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.
Cyhoeddwyd yn J Thromb Haemost (2015)

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
Cyhoeddwyd 2014

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
Cyhoeddwyd yn Mol Psychiatry (2016)

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
Cyhoeddwyd yn Mol Psychiatry (2015)

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. 
Cyhoeddwyd 2007