The distribution of constitutional and somatic mutations in the neurofibromatosis 2 gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference66 articles.
1. Micro-deletions and micro-insertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity;Ball;Hum Mutat,2005
2. Predictors of the risk of mortality in neurofibromatosis 2;Baser;Am J Hum Genet,2002
3. Evaluation of clinical diagnostic criteria for neurofibromatosis 2;Baser;Neurology,2002
4. Genotype-phenotype correlations for cataracts in neurofibromatosis 2;Baser;J Med Genet,2003
5. Genotype-phenotype correlations for nervous system tumors in neurofibromatosis 2: a population-based study;Baser;Am J Hum Genet,2004
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