Misleading linkage results in an NF2 presymptomatic test owing to mosaicism.

Author:

Bijlsma E K,Wallace A J,Evans D G

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis;Kanter, W.R.; Eldridge, R.; Fabricant, R.; Allen, J.C.; Koerber, T.;Neurology,1980

2. A clinical study of type 2 neurofibromatosis;Evans, D.G.R.; Huson, S.M.; Donnai, D.,1992

3. Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity;Parry, D.M.; Eldridge, R.; Kaiser-Kupfer, M.I.; Bouzas, E.A.; Pikus, A.; Patronas, N.;Am J Med Genet,1994

4. Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma;Seizinger, B.R.; Martuza, R.L.; Gusella, J.F.;Nature,1986

5. Genetic linkage analysis of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22;Rouleau, G.; Wertelecki, W.; Haines, J.L.;Nature,1987

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