(Q41547229)

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Von Hippel-Lindau syndrome: hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene

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Europe PubMed Central

3 October 2017

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Europe PubMed Central

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Von Hippel-Lindau syndrome: hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene (English)

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Europe PubMed Central

3 October 2017

J S Humphrey

1

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Europe PubMed Central

PubMed ID

9239471

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3 October 2017

R D Klausner

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2

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Europe PubMed Central

PubMed ID

9239471

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3 October 2017

W M Linehan

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3

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Europe PubMed Central

PubMed ID

9239471

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3 October 2017

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1 January 1996

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Europe PubMed Central

3 October 2017

Cancer Treatment and Research

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Europe PubMed Central

3 October 2017

88

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Europe PubMed Central

3 October 2017

13-39

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Europe PubMed Central

3 October 2017

Mutations of the VHL tumour suppressor gene in renal carcinoma

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24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NG0594-85

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10.1007/978-1-4615-6343-3_2

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PubMed ID

9239471

1 reference

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Europe PubMed Central

PubMed ID

9239471

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3 October 2017

(Q41547229)

Von Hippel-Lindau syndrome: hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene

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