1. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17;Barker, D.; Wright, E.; Nguyen, K.; Cannon, L.; Fain, P.; Goldgar, D.;Sccience,1987
2. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22;Rouleau, G.A.; Wertelecki, W.; Haines, J.L.; Hobbs, W.J.; Trofatter, J.A.; Seizinger, B.R.;Nature
3. National Institutes of Health Consensus Development Conference on Neurofibromatosis: Conference Statement. Arch Neurol 1988; 45: 575-8.
4. Eye findings in bilateral acoustic (central) neurofibromatosis: association with presenile lens opacities and cataracts but absence of Lisch nodules;Pearson-Webb, M.A.; Kaiser-Kupfer, M.I.; Eldridge, R.;N Englj Med,1986
5. The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2;Kaiser-Kupfer, M.; Freidlin, V.; Datiles, M.B.; Edwards, P.A.; Parry, Sherman J.L.; D.;Arch Ophthalmol,1989