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Neuroreport|May 1, 1993
Denervation impairs cutaneous microvascular function and blister healing in the rat hindlimbR W Carr, C A Delaney, R A Westerman, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardationH Jin, R J Gardner, R Viswesvaraiah, et al.
The European Respiratory Journal|November 1, 1996
Capsaicin cough receptor sensitivity test in childrenA B Chang, P D Phelan, R G Roberts, et al.
Genetic Testing|January 1, 1997
Dystrophin point mutation screening using a multiplexed protein truncation testN V Whittock, R G Roberts, C G Mathew, et al.
Human Genetics|November 10, 2001
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?T P Kerr, C A Sewry, S A Robb, et al.
Archives of Family Medicine|December 1, 1994
The advanced life support in obstetrics course. A national program to enhance obstetric emergency skills and to support maternity care practiceJ W Beasley, J R Damos, R G Roberts, et al.
Genomics|November 24, 1999
The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteinsH Jin, E Kendall, T C Freeman, et al.
Human Mutation|January 1, 1995
Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardationS Tuffery, U Lenk, R G Roberts, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 23, 2001
Bipartite interaction between neurofibromatosis type I protein (neurofibromin) and syndecan transmembrane heparan sulfate proteoglycansY P Hsueh, A M Roberts, M Volta, et al.
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