A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling.

Author:

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

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene;Seizinger, B.R.; Rouleau, G.A.; Ozelius, L.G.;Cell,1987

2. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17;Barker, D.; Wright, E.; Nguyen, K.;Science,1987

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

4. Genetic linkage analysis of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22;Rouleau, G.; Seizinger, B.R.; Ozelius, L.G.;Nature,1987

5. Health Consensus Development Conference Statement on Neurofibromatosis;National Institutes of;Neurofibromatosis Res Newsl,1987

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