Letter: Delayed drug-induced dystonias.

ανά Simpson, M A
Έκδοση 1973

Letter: An easy death--an uneasy argument.

ανά Simpson, M A
Έκδοση 1975

Future of British psychiatrists.

ανά Simpson, M A
Έκδοση 1971

Overseas students.

ανά Simpson, M. A.
Έκδοση 1967

Living with the dying.

ανά Simpson, M. A.
Έκδοση 1977

Female genital self-mutilation as a cause of vaginal bleeding

ανά Simpson, M. A., Anstee, B. H.
Έκδοση 1974

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

ανά Simpson, M A, Squires, T J, Busuttil, A
Έκδοση 2000

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

ανά Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Τόπος έκδοσης Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

ανά 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
Τόπος έκδοσης Mol Psychiatry (2018)

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

ανά 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.
Τόπος έκδοσης J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

ανά 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
Έκδοση 2014

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

ανά 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
Τόπος έκδοσης Mol Psychiatry (2016)

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

ανά 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
Τόπος έκδοσης Mol Psychiatry (2015)

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

ανά 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. 
Έκδοση 2007