6 results on '"Menko, F H"'
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2. Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
3. Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA 1/2-test results
4. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
5. Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes
6. Genetic defects underlying Peutz–Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
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