A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.

Author:

Evans D G,Huson S M,Donnai D,Neary W,Blair V,Teare D,Newton V,Strachan T,Ramsden R,Harris R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. Case of tumours in the skull, dura mater, and brain;Wishart, J.H.;Edinburgh Med Surg, J

2. Ueber die multiplenfibroma der haut und ihre beziehung zu den multiplen neuromen;F, Von Recklinghausen,1882

3. Bilateral acoustic neurofibromas: a clinical study and field survey of a family of five generations with bilateral deafness in thirty eight members;Gardner, W.J.; Frazier, C.H.;Arch Neurol Psychiatr

4. A clinical, pathological and genetic study of multiple neurofibromatosis;Crowe, F.W.; Schull, W.J.; Neal, J.V.,1956

5. 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

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