CrossRef Text and Data Mining
Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining.
A Very Aggressive Hemangioblastomatosis Without VHL Gene Mutation
Jeong Goo Park, Sang Woo Song, Young-Cho Koh
The Nerve. 2015;1(1):44-46.   Published online 2015 October 31    DOI: https://doi.org/10.21129/nerve.2015.1.1.44

Excel Download

A Very Aggressive Hemangioblastomatosis Without VHL Gene Mutation
The Nerve. 1970;1(1):44-46   Crossref logo
Link1 Link2

MP71-15 VHL GENE MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE CORRELATIONSHIP OF CHINESE VHL PATIENTS
Journal of Urology. 2016;195(4S):   Crossref logo
Link1 Link2 Link3

Comprehensive characterization of Alu ÔÇÉmediated breakpoints in germline VHL gene deletions and rearrangements in patients from 71 VHL families
Human Mutation. 2021;42(5):520-529   Crossref logo
Link1 Link2 Link3

Role of VHL gene mutation in human renal cell carcinoma
Tumor Biology. 2011;33(1):9-16   Crossref logo
Link1 Link2 Link3

Gene array of VHL mutation and hypoxia shows novel hypoxia-induced genes and that cyclin D1 is a VHL target gene
British Journal of Cancer. 2004;90(6):1235-1243   Crossref logo
Link1 Link2 Link3

Abstract #130 A Case of Pheochromocytoma Associated with Never Reported Rare New Mutation of VHL Gene
Endocrine Practice. 2018;24:18   Crossref logo
Link1 Link2

A c.464T>A mutation in VHL gene in a Chinese family with VHL syndrome
Journal of Neuro-Oncology. 2012;111(3):313-318   Crossref logo
Link1 Link2 Link3

Response to: Extremely low risk of pheochromocytomas in complete VHL gene deletion cases
Human Mutation. 2009;30(9):1367-1367   Crossref logo
Link1 Link2

Primary peritoneal epithelioid mesothelioma of clear cell type with a novel VHL gene mutation: a case report
Human Pathology. 2019;83:199-203   Crossref logo
Link1 Link2

Germline Mutation of von Hippel-Lindau (VHL) Gene 695 G>A (R161Q) in a Patient with a Peculiar Phenotype with Type 2C VHL Syndrome
Annals of the New York Academy of Sciences. 2006;1073(1):198-202   Crossref logo
Link1 Link2

This metadata service is kindly provided by CrossRef from May 29, 2014. Nerve has participated in CrossRef Text and Data Mining service since October 29, 2014.