scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.UROLOGY.2013.09.069 |
P698 | PubMed publication ID | 24581539 |
P50 | author | Yu Fan | Q87834654 |
P2093 | author name string | Ning Zhang | |
Xi Wang | |||
Dingfang Bu | |||
Kan Gong | |||
Pengjie Wu | |||
Shuanghe Peng | |||
Teng Li | |||
Xianghui Ning | |||
P2860 | cites work | Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus | Q28242901 |
Identification of the von Hippel-Lindau disease tumor suppressor gene | Q29618644 | ||
Central nervous system lesions in von Hippel-Lindau syndrome | Q33591720 | ||
Von Hippel-Lindau disease: a genetic study | Q33597245 | ||
A genetic register for von Hippel-Lindau disease | Q33683199 | ||
LINDAU'S DISEASE. REVIEW OF THE LITERATURE AND STUDY OF A LARGE KINDRED. | Q34540867 | ||
High frequency of novel germline mutations in the VHL gene in the heterogeneous population of Brazil | Q41876493 | ||
Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families | Q43466454 | ||
Clinical and mutation analysis of four Chinese families with von Hippel-Lindau disease | Q44819707 | ||
Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients | Q44847037 | ||
Molecularly genetic analysis of von Hippel-Lindau associated central nervous system hemangioblastoma. | Q45966988 | ||
A c.464T>a mutation in VHL gene in a Chinese family with VHL syndrome | Q46133879 | ||
Familial and genetic researches on three Chinese families with von Hippel-Lindau disease | Q46169843 | ||
Mosaicism in von Hippel-Lindau disease with severe renal manifestations. | Q53121842 | ||
Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family. | Q53311772 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | von Hippel-Lindau disease | Q741315 |
P304 | page(s) | 675.e1-5 | |
P577 | publication date | 2014-03-01 | |
P1433 | published in | Urology | Q7900884 |
P1476 | title | Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients. | |
P478 | volume | 83 |
Q47362904 | Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma |
Q41754374 | Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families. |
Q38964723 | Profilin1 biology and its mutation, actin(g) in disease |
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