Search Results - Simpson, M A

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  1. 1
    Letter: Delayed drug-induced dystonias.

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

    Published 1973
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  2. 2
    Letter: An easy death--an uneasy argument.

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

    Published 1975
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  3. 3
    Future of British psychiatrists.

    Future of British psychiatrists. by Simpson, M A

    Published 1971
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  4. 4
    Overseas students.

    Overseas students. by Simpson, M. A.

    Published 1967
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  5. 5
    Living with the dying.

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

    Published 1977
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  6. 6
    Female genital self-mutilation as a cause of vaginal bleeding

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

    Published 1974
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  7. 7
    The case of Jane Anderson, Portobello, 1889-1914.

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

    Published 2000
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  8. 8
    New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy

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

    Published 2016
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  9. 9
    A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

    Published 2012
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  10. 10
    A genome-wide association study for extremely high intelligence

    A genome-wide association study for extremely high intelligence by 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

    Published 2018
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  11. 11
    Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

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

    Published 2015
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  12. 12
    Germline CDH1 mutations in bilateral lobular carcinoma in situ

    Germline CDH1 mutations in bilateral lobular carcinoma in situ by 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

    Published 2014
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  13. 13
    Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

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

    Published 2015
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  14. 14
    Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development

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

    Published 2007
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