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Journal of Medical Genetics|October 10, 1997
Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndromeM W Partington, K Fagan, V Soubjaki, et al.
Clinical Genetics|June 18, 2004
Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARXM W Partington, G Turner, J Boyle, et al.
Canadian Medical Association Journal|April 9, 1977
Typhoid outbreak in Kingston, Ont: experience with high-dose oral ampicillinG Hardy, C J Padfield, P Chadwick, et al.
Clinical Genetics|January 1, 1990
A new syndrome of familial short stature, small hands, valvular heart disease and a characteristic faciesF A Collins, M W Partington, D Mulcahy, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31)A J Donnelly, M W Partington, A K Ryan, et al.
Canadian Medical Association Journal|February 15, 1981
Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatmentM W Partington, W R Ghent, E V Sears, et al.
American Journal of Medical Genetics|May 1, 1988
A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pterM W Partington, J C Mulley, G R Sutherland, et al.
American Journal of Medical Genetics|August 1, 1994
Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosisA K Gedeon, J C Mulley, H Kozman, et al.
Canadian Medical Association Journal|October 9, 1971
Surdo-cardiac syndrome: incidence among children in schools for the deafJ E Fay, P M Olley, M W Partington, et al.
American Journal of Human Genetics|September 1, 1983
Additional evidence for fragile X activity in heterozygous carriersI A Uchida, V C Freeman, H Jamro, et al.
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