Schizophrenia and Affective Disorders—Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and P300 Findings in a Family
Blackwood, D.H.R., Fordyce, A., Walker, M.T., St. Clair, D.M., Porteous, D.J., Muir, W.J.
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Published in American journal of human genetics (01.08.2001)
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Twin zygosity testing for medical purposes
St. Clair, D.M, St. Clair, J.B, Swainson, O.P, Bamforth, F, Machin, G.A
Published in Journal of clinical forensic medicine (01.09.1999)
Published in Journal of clinical forensic medicine (01.09.1999)
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Schizophrenia: A neuropsychiatric phenotype of the Usher syndrome type III allele
Sharp, C.W., Muir, W.J., Blackwood, D.H.R., Walker, M., Gosden, C., St. Clair, D.M.
Published in Schizophrenia research (01.04.1993)
Published in Schizophrenia research (01.04.1993)
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Segregation analysis of complex phenotypes: An application to schizophrenia and auditory P300 latency
Sham, P.C., Morton, N.E., Muir, W.J., Walker, M., Collins, A., Shields, D.C., St. Clair, D.M., Blackwood, D.H.R.
Published in Schizophrenia research (01.04.1993)
Published in Schizophrenia research (01.04.1993)
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Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia
Muir, W J, Gosden, C M, Brookes, A J, Fantes, J, Evans, K L, Maguire, S M, Stevenson, B, Boyle, S, Blackwood, D H, St Clair, D M
Published in Cytogenetics and cell genetics (01.01.1995)
Published in Cytogenetics and cell genetics (01.01.1995)
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