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American Journal of Medical Genetics|January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in malesM W Partington, P J Marriott, R S Prentice, et al.American Journal of Medical Genetics|May 1, 1988
A new syndrome with mental retardation, short stature and an Xq duplicationA Thode, M W Partington, M Y Yip, et al.American Journal of Medical Genetics|May 1, 1988
X-linked mental retardation with dystonic movements of the handsM W Partington, J C Mulley, G R Sutherland, et al.Journal of Neurogenetics|June 1, 1985
The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implicationsC J Forster-Gibson, L M Mulligan, M W Partington, et al.American Journal of Medical Genetics|August 1, 1983
Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twinsJ G Hall, S D Reed, B C McGillivray, et al.American Journal of Medical Genetics|October 15, 1994
Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1M J Edwards, C J Challinor, P W Colley, et al.Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.Genomics|August 1, 1994
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneV Biancalana, E Trivier, C Weber, et al.Nature Genetics|August 1, 1992
Fragile X syndrome without CCG amplification has an FMR1 deletionA K Gedeon, E Baker, H Robinson, et al.American Journal of Medical Genetics|February 1, 1993
Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28L C Adès, A K Gedeon, M J Wilson, et al.Pageof 5