Works matching IS 13899600 AND DT 2005 AND VI 4 AND IP 1
Results: 12
Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx.
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- Familial Cancer, 2005, v. 4, n. 1, p. 17, doi. 10.1007/s10689-004-5740-1
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- Article
SDHC mutations in hereditary paraganglioma/pheochromocytoma.
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- Familial Cancer, 2005, v. 4, n. 1, p. 9, doi. 10.1007/s10689-004-0621-1
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- Article
Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic features.
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- Familial Cancer, 2005, v. 4, n. 1, p. 37, doi. 10.1007/s10689-004-5347-6
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Instructions for Authors.
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- Familial Cancer, 2005, v. 4, n. 1, p. 69, doi. 10.1007/s10689-005-4128-1
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- Article
Mutations of the SDHB and SDHD genes.
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- Familial Cancer, 2005, v. 4, n. 1, p. 49, doi. 10.1007/s10689-004-4227-4
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- Article
Pheochromocytoma in von HippelLindau disease and neurofibromatosis type 1.
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- Familial Cancer, 2005, v. 4, n. 1, p. 13, doi. 10.1007/s10689-004-6128-y
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Multiple endocrine neoplasia type 2.
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- Familial Cancer, 2005, v. 4, n. 1, p. 25, doi. 10.1007/s10689-005-0656-y
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- Article
Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications.
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- Familial Cancer, 2005, v. 4, n. 1, p. 43, doi. 10.1007/s10689-004-1327-0
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- Article
Pheochromocytoma where are we? Where should we go? A medical and scientific odyssey.
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- Familial Cancer, 2005, v. 4, n. 1, p. 1, doi. 10.1007/s10689-004-0620-2
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- Article
Paragangliomas of the head and neck: diagnosis and treatment.
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- Familial Cancer, 2005, v. 4, n. 1, p. 55, doi. 10.1007/s10689-004-2154-z
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- Article
Molecular pathogenesis of MEN2-associated tumors.
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- Familial Cancer, 2005, v. 4, n. 1, p. 3, doi. 10.1007/s10689-004-7022-3
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- Article
Imaging of pheochromocytoma and paraganglioma.
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- Familial Cancer, 2005, v. 4, n. 1, p. 61, doi. 10.1007/s10689-004-2155-y
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- Article