9 results on '"Menko, F H"'
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2. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
3. Highly variable clinical manifestations in a large family with a novel GATA2 mutation
4. Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
5. Absence of the Birt–Hogg–Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility
6. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
7. Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2
8. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications
9. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications
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