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Archives of Disease in Childhood|February 1, 1993
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspectsW Reardon, R Newcombe, I Fenton, et al.Current Medicinal Chemistry|December 4, 2018
Transition Metal-Based Prodrugs for Anticancer Drug DeliveryAna M F Phillips, Armando J L PombeiroClinical Genetics|November 1, 1986
Marfan syndrome: exclusion of genetic linkage to the COL1A2 geneP Tsipouras, A L Børresen, S Bamforth, et al.Annals of Human Genetics|May 1, 1983
Genetic linkage between the loci for myotonic dystrophy and peptidase DT O'Brien, S Ball, M Sarfarazi, et al.Community Genetics|February 13, 2004
The frequency of inherited disorders database: prevalence of Huntington diseaseL N Al-Jader, P S Harper, M Krawczak, et al.Muscle & Nerve|May 1, 1991
Assessment of locomotor function in young boys with Duchenne muscular dystrophyR A Smith, R G Newcombe, J R Sibert, et al.Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.Journal of Medical Genetics|August 1, 1989
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesM Upadhyaya, M Sarfarazi, P W Lunt, et al.Human Molecular Genetics|April 18, 1998
Huntingtin interacts with cystathionine beta-synthaseJ M Boutell, J D Wood, P S Harper, et al.Human Genetics|April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localizationA Clarke, M Sarfarazi, N S Thomas, et al.Pageof 23