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Muscle & Nerve. Supplement|April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.Archives of Disease in Childhood|September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)P E Jardine, M C Koch, P W Lunt, et al.Muscle & Nerve. Supplement|January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.Diagnostic Microbiology and Infectious Disease|August 1, 1997
Serum inhibitory titers and serum bactericidal titers for human subjects receiving multiple doses of the antibacterial oxazolidinones eperezolid and linezolidR D Schaadt, D H Batts, P T Daley-Yates, et al.Human Molecular Genetics|May 1, 1995
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)P W Lunt, P E Jardine, M C Koch, et al.Journal of Medical Genetics|March 1, 1994
Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysisP E Jardine, P D Cotter, S A Johnson, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 2, 2007
Mosaicism in autosomal dominant polycystic kidney disease revealed by genetic testing to enable living related renal transplantationA Connor, P W Lunt, C Dolling, et al.Archives of Disease in Childhood|March 6, 1998
An unusually severe phenotype for familial adenomatous polyposisD M Eccles, P W Lunt, Y Wallis, et al.Archives of Disease in Childhood|May 27, 2003
22q11 deletion: a multisystem disorder requiring multidisciplinary inputK L Greenhalgh, I A Aligianis, G Bromilow, et al.Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.Pageof 6