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Genes, Chromosomes & Cancer|April 30, 1999
DNA studies underestimate the major role of CDKN2A inactivation in oral and oropharyngeal squamous cell carcinomasC L Wu, L Roz, S McKown, et al.Journal of Medical Genetics|March 1, 1993
Mapping of the X linked form of hyper IgM syndrome (HIGM1)M Padayachee, R J Levinsky, C Kinnon, et al.Journal of Medical Genetics|May 1, 1989
Neural tube defect recurrence after 'partial' vitamin supplementationS Sheppard, N C Nevin, M J Seller, et al.Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.Human Genetics|May 1, 1992
Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD)B Müller, C Dechant, G Meng, et al.Somatic Cell and Molecular Genetics|September 1, 1991
New DNA markers in the Huntington's disease gene candidate regionC S Lin, M Altherr, G Bates, et al.Lancet (London, England)|May 7, 1983
Further experience of vitamin supplementation for prevention of neural tube defect recurrencesR W Smithells, N C Nevin, M J Seller, et al.Archives of Disease in Childhood|May 1, 1986
Recurrent neural tube defects, risk factors and vitaminsJ Wild, A P Read, S Sheppard, et al.The British Journal of Dermatology|December 21, 2004
Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic studyC Hewitt, C-L Wu, F N Hattab, et al.Genomics|October 1, 1990
Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets familiesR V Thakker, K E Davies, A P Read, et al.Pageof 10