173 related articles for article (PubMed ID: 19806577)
1. [Large germline deletion of the VHL gene in Chinese families with von Hippel-Lindau syndrome].
Zhang J; Chen HG; Xue W; Zhou LX; Huang YR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):539-41. PubMed ID: 19806577
[TBL] [Abstract][Full Text] [Related]
2. Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families.
Zhang J; Huang Y; Pan J; Liu D; Zhou L; Xue W; Chen Q; Dong B; Xuan H
J Cancer Res Clin Oncol; 2008 Nov; 134(11):1211-8. PubMed ID: 18446368
[TBL] [Abstract][Full Text] [Related]
3. 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.
Wu P; Zhang N; Wang X; Ning X; Li T; Bu D; Gong K
J Hum Genet; 2012 Apr; 57(4):238-43. PubMed ID: 22357542
[TBL] [Abstract][Full Text] [Related]
4. VHL Germline Mutations in Argentinian Patients with Clinical Diagnoses or Single Typical Manifestations of Type 1 von Hippel-Lindau Disease.
Mathó C; Sansó G; Diez B; Barontini M; Pennisi PA
Genet Test Mol Biomarkers; 2016 Dec; 20(12):771-776. PubMed ID: 27617348
[TBL] [Abstract][Full Text] [Related]
5. [Germ line mutations in Chinese kindreds with von Hippel-Lindau syndrome].
Zhang J; Huang YR; Pan JH; Liu DM; Zhou LX; Xue W; Chen Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):124-7. PubMed ID: 17407064
[TBL] [Abstract][Full Text] [Related]
6. Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel-Lindau disease: case report.
Liu Z; Zhou J; Li L; Yi Z; Lu R; Li C; Gong K
BMC Med Genet; 2020 Oct; 21(1):191. PubMed ID: 33004005
[TBL] [Abstract][Full Text] [Related]
7. Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) gene.
Hes F; Zewald R; Peeters T; Sijmons R; Links T; Verheij J; Matthijs G; Leguis E; Mortier G; van der Torren K; Rosman M; Lips C; Pearson P; van der Luijt R
Hum Genet; 2000 Apr; 106(4):425-31. PubMed ID: 10830910
[TBL] [Abstract][Full Text] [Related]
8. Germline mutations of the VHL gene in seven Chinese families with von Hippel-Lindau disease.
Huang Y; Zhou D; Liu J; Zhou P; Li X; Wang Z
Int J Mol Med; 2012 Jan; 29(1):47-52. PubMed ID: 21972040
[TBL] [Abstract][Full Text] [Related]
9. Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients.
Wang X; Zhang N; Ning X; Li T; Wu P; Peng S; Fan Y; Bu D; Gong K
Urology; 2014 Mar; 83(3):675.e1-5. PubMed ID: 24581539
[TBL] [Abstract][Full Text] [Related]
10. Detection of germline deletions using real-time quantitative polymerase chain reaction in Japanese patients with von Hippel-Lindau disease.
Hattori K; Teranishi J; Stolle C; Yoshida M; Kondo K; Kishida T; Kanno H; Baba M; Kubota Y; Yao M
Cancer Sci; 2006 May; 97(5):400-5. PubMed ID: 16630138
[TBL] [Abstract][Full Text] [Related]
11. Germline mutation of Glu70Lys is highly frequent in Korean patients with von Hippel-Lindau (VHL) disease.
Hwang S; Ku CR; Lee JI; Hur KY; Lee MS; Lee CH; Koo KY; Lee JS; Rhee Y
J Hum Genet; 2014 Sep; 59(9):488-93. PubMed ID: 25078357
[TBL] [Abstract][Full Text] [Related]
12. De novo VHL germline mutation detected in a patient with mild clinical phenotype of von Hippel-Lindau disease.
Ding X; Zhang C; Frerich JM; Germanwala A; Yang C; Lonser RR; Mao Y; Zhuang Z; Zhang M
J Neurosurg; 2014 Aug; 121(2):384-386. PubMed ID: 24678776
[TBL] [Abstract][Full Text] [Related]
13. Clinical and mutation analysis of four Chinese families with von Hippel-Lindau disease.
Chen J; Geng W; Zhao Y; Zhao H; Wang G; Huang F; Liu F; Geng X
Clin Transl Oncol; 2013 May; 15(5):391-7. PubMed ID: 23143947
[TBL] [Abstract][Full Text] [Related]
14. Genetic study of a large Chinese kindred with von Hippel-Lindau disease.
Huang YR; Zhang J; Wang JD; Fan XD
Chin Med J (Engl); 2004 Apr; 117(4):552-7. PubMed ID: 15109448
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive characterization of Alu-mediated breakpoints in germline VHL gene deletions and rearrangements in patients from 71 VHL families.
Vocke CD; Ricketts CJ; Schmidt LS; Ball MW; Middelton LA; Zbar B; Linehan WM
Hum Mutat; 2021 May; 42(5):520-529. PubMed ID: 33675279
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype correlations in VHL exon deletions.
McNeill A; Rattenberry E; Barber R; Killick P; MacDonald F; Maher ER
Am J Med Genet A; 2009 Oct; 149A(10):2147-51. PubMed ID: 19764026
[TBL] [Abstract][Full Text] [Related]
17. Familial and genetic researches on three Chinese families with von Hippel-Lindau disease.
Mao XC; Su ZP; Yu WQ; Zheng WM; Zeng YJ
Neurol Res; 2009 Sep; 31(7):743-7. PubMed ID: 19133167
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel duplication mutation in the VHL gene in a large Chinese family with Von Hippel-Lindau (VHL) syndrome.
Cao LH; Kuang BH; Chen C; Hu C; Sun Z; Chen H; Wang SS; Luo Y
Genet Mol Res; 2014 Dec; 13(4):10177-83. PubMed ID: 25501229
[TBL] [Abstract][Full Text] [Related]
19. Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.
Gomy I; Molfetta GA; de Andrade Barreto E; Ferreira CA; Zanette DL; Casali-da-Rocha JC; Silva WA
Fam Cancer; 2010 Dec; 9(4):635-42. PubMed ID: 20567917
[TBL] [Abstract][Full Text] [Related]
20. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
Gergics P; Patocs A; Toth M; Igaz P; Szucs N; Liko I; Fazakas F; Szabo I; Kovacs B; Glaz E; Racz K
Eur J Endocrinol; 2009 Sep; 161(3):495-502. PubMed ID: 19574279
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]