1. Cornelia de Lange syndrome in several members of the same family;Kumar, D.; Blank, C.E.; Griffiths, B.L.;J Med Genet,1985
2. A new familial syndrome with osseous dysplasia and mental deficiency;Ruvalcaba, R.H.A.; Reichert, A.; Smith, D.W.;J Pediatr,1971
3. A computerised data base for the diagnosis of rare dysmorphic syndromes;Winter, R.M.; Baraitser, M.; Douglas, J.M.;J Med Genet,1984
4. A study of retinitis pigmentosa in the City of Birmingham. I Prevalence;SIR, Reference Bundey S.; SJ, Crews;II Clinical and genetic heterogeneity. J Med Genet,1984
5. Med Genet 1985; 22: 104-1 1) are to be congratulated on their thorough study of perinatally lethal renal disease. Of interest, with regard to the group classified by them as multiple defects, is our case;Bankier