Genetic alterations and histopathologic findings in familial renal cell carcinoma

Publication:
Genetic alterations and histopathologic findings in familial renal cell carcinoma

dc.contributor.author	Hansel, D.E	es
dc.date.accessioned	2011-06-30T12:02:37Z
dc.date.available	2011-06-30T12:02:37Z
dc.date.issued	2006
dc.description.abstract	Renal cell carcinoma is increasing in frequency in the United States and is often detected late in the course of disease due to nonspecific symptoms. A subset of renal cell carcinoma is attributable to familial or hereditary syndromes, including von Hippel-Lindau and Birt-Hogg-Dubé syndromes, among others. Understanding of the molecular alterations in patients with familial syndromes may provide some insight into the underlying mechanisms of disease initiation and progression. This review describes the various subtypes of renal cell carcinoma and the familial syndromes associated with these tumors.	es
dc.format	application/pdf	es
dc.format.extent	8	es
dc.identifier.issn	0213-3911	es
dc.identifier.uri	http://hdl.handle.net/10201/22643
dc.language	eng	es
dc.publisher	Murcia : F. Hernández	es
dc.relation.ispartof	Histology and histopathology	es
dc.rights	info:eu-repo/semantics/openAccess	es
dc.subject	Kidney cancer	es
dc.subject	Pathology	es
dc.subject.other	CDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología::616.6 - Patología del sistema genitourinario	es
dc.title	Genetic alterations and histopathologic findings in familial renal cell carcinoma	es
dc.type	info:eu-repo/semantics/article	es
dspace.entity.type	Publication	es

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