Search Results (16)
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MatchTypeWhy
Neoplastic Syndromes, HereditaryConcept Why?
Chromophobe renal cell carcinoma in a patient with the Birt-Hogg-Dube syndrome.Academic Article Why?
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).Academic Article Why?
Homeosis and polyposis: a tale from the mouse.Academic Article Why?
Italian family with two independent mutations: 3358T/A in BRCA1 and 8756delA in BRCA2 genes.Academic Article Why?
More than just skin deep: faciocutaneous clues to genetic syndromes with malignancies.Academic Article Why?
MSH-6: extending the reliability of immunohistochemistry as a screening tool in Muir-Torre syndrome.Academic Article Why?
Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis.Academic Article Why?
Tseng, JenniferPerson Why?
Hoffman, JodiPerson Why?
Carsillo, ThomasPerson Why?
Thiagalingam, SamPerson Why?
Pheochromocytoma and paraganglioma: imaging characteristics.Academic Article Why?
Vinceti, MarcoPerson Why?
Ng, LindaPerson Why?
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  • Hereditary Cancer Syndromes
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