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American Journal of Medical Genetics|September 1, 1983
Carrier detection in Hunter syndromeI M Archer, I D Young, D W Rees, et al.Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.Journal of Medical Genetics|February 1, 1986
Gene mapping and chromosome 19D J Shaw, J D Brook, A L Meredith, et al.Human Genetics|December 1, 1986
Localisation of the gene for Hunter syndrome on the long arm of X chromosomeM Upadhyaya, M Sarfarazi, J S Bamforth, et al.Brain : a Journal of Neurology|December 1, 1986
Cerebellar haemangioblastoma and von Hippel-Lindau diseaseS M Huson, P S Harper, M D Hourihan, et al.Journal of Medical Genetics|September 1, 1995
Characterisation of germline mutations in the neurofibromatosis type 1 (NF1) geneM Upadhyaya, J Maynard, M Osborn, et al.Journal of Medical Genetics|February 1, 1986
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophyS M Huson, A L Meredith, M Sarfarazi, et al.American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Nocturnal oxygenation and prognosis in Duchenne muscular dystrophyM F Phillips, P E Smith, N Carroll, et al.Archives of Disease in Childhood|March 1, 1991
Leukaemia mortality among relatives of cystic fibrosis patientsL N al-Jader, R R West, J A Holmes, et al.Nucleic Acids Research|April 25, 1983
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosomeK E Davies, P L Pearson, P S Harper, et al.Pageof 23