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Physics in Medicine and Biology|October 21, 2017
A method for acquiring random range uncertainty probability distributions in proton therapyS M Holloway, M D Holloway, S J ThomasJournal of Medical Genetics|April 1, 1990
Attitudes of general practitioners to presymptomatic testing for Huntington's diseaseM E Mennie, S M Holloway, D J BrockJournal of Epidemiology and Community Health|September 1, 1983
A family study of Paget's disease of boneJ A Sofaer, S M Holloway, A E EmeryScottish Medical Journal|March 12, 2010
Paediatric referral and attendance rates for the clinical genetics service in south-east Scotland--a comparison of a regional clinic with satellite clinicsS M Holloway, A K Lampe, W W K LamAnnals of Human Genetics|May 1, 1978
On effects of relaxed selection in familial disordersA M Davie, C Smith, R N Curnow, et al.Journal of Medical Genetics|March 1, 2007
Further evidence of the increased risk for malignant peripheral nerve sheath tumour from a Scottish cohort of patients with neurofibromatosis type 1J A McCaughan, S M Holloway, R Davidson, et al.Journal of the Neurological Sciences|July 1, 1994
Clinical heterogeneity of familial motor neuron disease: report of 11 pedigrees from a population based study in Scotland. The Scottish Motor Neuron Disease Research GroupA M Chancellor, H Fraser, R J Swingler, et al.Gene|October 31, 2000
Characterization of fimN, a new Bordetella bronchiseptica major fimbrial subunit geneS A Kania, S Rajeev, E H Burns, et al.Journal of Neurology|June 1, 1993
The prognosis of adult-onset motor neuron disease: a prospective study based on the Scottish Motor Neuron Disease RegisterA M Chancellor, J M Slattery, H Fraser, et al.Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Presymptomatic testing for Huntington's disease by linkage and by direct mutation analysis: comparison of uptake of testing and characteristics of test applicantsS M Holloway, M E Porteous, D R Fitzpatrick, et al.Pageof 3