A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic ricketsFiona Francis, Thomas Meitinger, Tim M. Strom et al.|Nature Genetics|1995Cited by 1.1k
Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysisAndrew Read, J. L. H. O’Riordan, Rajesh V. Thakker et al.|Human Genetics|1986Cited by 81
Norrie disease resulting from a gene deletion: clinical features and DNA studies.Dian Donnai, Andrew Read, R. Mountford|Journal of Medical Genetics|1988Cited by 67
The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)Peter Rowe, K E Davies, J.N. Goulding et al.|Human Genetics|1996Cited by 57
Bridging markers defining the map position of X linked hypophosphataemic rickets.Rajesh V. Thakker, Andrew King, Andrew Read et al.|Journal of Medical Genetics|1987Cited by 56