A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Author:

Huson S M,Compston D A,Harper P S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Gcne for von Rccklinghauscn ncurofibromatosis is in the pcricentromcric region of chromosome 17. Scientce 1987: 236: 1 10(0-2. - Scizingcr BR. Roulcau GA;K, Barker V.Wright E.Nguycn;Ozclius LG. et al. Genetic; linkage of von Recklinghauscn ncurofibromatosis to the ncrvc growth factor rcceptor genc

2. Multipoint linkage analysis in neurofibromatosis type 1: an international collaboration;Goldgar, D.E.; Green, P.; Parry, D.M.; Mulvihill, J.J.;Am J Hum Genet,1989

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

4. mutation rate, and effect of parental transmission on severity;Prevalence, fitness;J Med Genet,1989

5. Penetrance and variability of neurofibromatosis: a genetic study of 60 familics;Carey, J.C.; Laub, J.M.; Hall, B.D.;Birth Defects,1979

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