C. Meredith
University of Western Australia
9 Papers
204 Citations
C. Meredith is an academic researcher from University of Western Australia. The author has contributed to research in topics: Myopathy & Gene mapping. The author has an hindex of 8, co-authored 9 publications. Previous affiliations of C. Meredith include Edith Cowan University.
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Papers
Autosomal dominant distal myopathy: linkage to chromosome 14
Nigel G. Laing,B.A. Laing,C. Meredith,Steve D. Wilton,Frank L. Mastaglia,Peter Robbins,K. Honeyman,S. Dorosz,Byron Kakulas +8 more
- 01 Jan 1993
TL;DR: It is probable that a gene for distal myopathy, MPD1, is located on chromosome 14, which should allow other investigators studying distalmyopathy families to test this region for linkage in other types of the disease, to confirm linkage or to demonstrate the likely genetic heterogeneity.
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•Journal Article
Autosomal dominant distal myopathy: linkage to chromosome 14.
Nigel G. Laing,B.A. Laing,C. Meredith,Steve D. Wilton,Peter D. Robbins,K. Honeyman,S. Dorosz,H. Kozman,Frank L. Mastaglia,Byron Kakulas +9 more
TL;DR: In this paper, the authors studied a family with distal myopathy (MIM 160500) containing nine living affected individuals and found that the myopathy in this family is closest in clinical phenotype to that first described by Gowers in 1902.
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Early onset chromosome 14-linked distal myopathy (Laing)
Francis Mastaglia,Beverley A. Phillips,Lesley Cala,Lesley Cala,C. Meredith,C. Meredith,S. Egli,P.A. Akkari,Nigel G. Laing +8 more
TL;DR: The pattern of muscle involvement was similar to that in the 'tibial' forms of distal myopathy such as the Finnish (Udd) and Markesbery-Griggs types, with additional involvement of the finger extensors and of some more proximal limb and neck muscles.
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Autosomal dominant distal myopathy linkage on Chromosome 14
C. Meredith,B.A. Laing,Steve D. Wilton,Francis Mastaglia,Peter Robbins,H. Kozman,K. Honeyman,S. Dorosz,Byron Kakulas,Nigel G. Laing +9 more
- 01 Jan 1994
TL;DR: In this paper, the authors studied a family with distal myopathy (MIM 160500) containing nine living affected individuals and found that the myopathy in this family is closest in clinical phenotype to that first described by Gowers in 1902.
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Autosomal dominant distal myopathy not linked to the known distal myopathy loci
Kevin J. Felice,C. Meredith,C. Meredith,N. Binz,A. Butler,R. Jacob,P.A. Akkari,P.A. Akkari,Joachim Hallmayer,Nigel G. Laing +9 more
TL;DR: The clinical and pathological features appear distinct from other previously described but genetically-undetermined autosomal dominant distal myopathies, suggesting the existence of at least one moredistal myopathy locus.
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