HusonS.M., CompstonD.A.S., HarperP.S.A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counseling. J Med Genet1989; 26: 712–21.
7.
National Institutes of Health.Neurofibromatosis. Consensus Development Conference Statement. Washington, D.C., July 13–15, 1987.
8.
LubsM.L.E., BauerM.S., FormasM.E.Lisch nodules in neurofibromatosis type 1. NEJM1991; 324: 1264–6.
9.
CharlesS.J., MooreA.T., YatesJ.R.W.Lisch nodules in neurofibromatosis type 2. Arch Ophthalmol1989; 107: 1571–2.
10.
Kaiser-KupferM.I., FreidlinV., DatilesM.B.The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2. Arch Ophthalmol1989; 107: 541–4.
11.
RoosK.L., DunnD.W.Neurofibromatoses. CA - A Cancer Journal for Clinicians; in press.
12.
GoldgarD.E., GreenP., ParryD.M.Multipoint linkage analysis in neurofibromatosis type 1; an international collaboration. Am J Hum Genet1989; 44: 6–12.
13.
ParryD.M.Gene mapping and tumor genetics (pp 41–42), in Mulvihill JJ (moderator): Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis): an update. Ann Intern Med1990; 113: 39–52.
14.
LedbetterD.H., RichD.C., O'ConnellP.Precise localization of NF-1 to 17 q 11.2 by balanced translocation. Am J Hum Genet1989; 44: 20–24.
15.
BuchbergA.M., BedigianH.G., TaylorB.A.Localization of Evi-2 to chromosome 11: linkage to other proto-oncogene and growth factor loci using interspecific backcross mice. Oncogene Res1988; 2: 149–65.
16.
IccardiV.M.Neurofibromatosis: past, present, and future. NEJM1991; 324: 1283–5.
17.
XuG., O'ConnellP., ViskochilD.The neurofibromatosis type 1 gene encodes a protein related to GAP. Cell1990; 62: 599–608.
18.
The Neurofibromatoses: From clinical phenotypes to the genes.American Academy of Neurology, April 26, 1991, Boston, MA.
19.
SeizingerB.R., MartuzaR.L., GusellaJ.F.Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature1986; 322: 644–7.
20.
SeizingerB.R., RouleauG., OzeliusL.J.Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis. Science1987; 236: 317–19.
21.
RouleauG.A., WerteleckiW., HainesJ.L.Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. Nature1987; 329(6136): 246–8.
22.
WerteleckiW., RouleauG.A., SupernauD.W.Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred. N Engl J Med1988; 319: 278–83.
23.
MiyamotoR.T., RoosK.L., CampbellR.L.Contemporary management of neurofibromatosis. Ann Otol Rhinol Laryngol1991; 100: 38–43.
MiyamotoR.T., CampbellR.L., FritschM.Preservation of hearing in neurofibromatosis 2. Otolaryngol Head Neck Surg1990; 103: 619–24.
26.
MiyamotoR.T., RoosK.L., CampbellR.L.Hearing preservation in Neurofibromatosis-2 (Abstract 167), in Program and Abstracts of the Copenhagen Acoustic Neuroma Conference. Copenhagen Denmark, August 1991.
27.
MiyamotoR.T., RoosK.L., CampbellR.L.Hearing preservation in Neurofibromatosis-2, in Proceedings of the First International Skull Base Congress, Hannover, Germany, June 14–20, 1992; in press.