Richard S - Search Results

1

Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene.

Cybulski C, Krzystolik K, Maher ER, Richard S, Kurzawski G, Gronwald J, Lubiński J. Cybulski C, et al. Among authors: richard s. Hum Genet. 1999 Oct;105(4):333-6. doi: 10.1007/s004399900137. Hum Genet. 1999. PMID: 10543401

2

DNA-based presymptomatic diagnosis for the von Hippel-Lindau disease by linkage analysis.

Olschwang S, Boisson C, Richard S, Resche F, Thomas G. Olschwang S, et al. Among authors: richard s. Eur J Hum Genet. 1995;3(2):108-15. doi: 10.1159/000472284. Eur J Hum Genet. 1995. PMID: 7552140

3

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.

Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al. Zbar B, et al. Among authors: richard s. Hum Mutat. 1996;8(4):348-57. doi: 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3. Hum Mutat. 1996. PMID: 8956040

4

Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.

Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER. Prowse AH, et al. Among authors: richard s. Am J Hum Genet. 1997 Apr;60(4):765-71. Am J Hum Genet. 1997. PMID: 9106522 Free PMC article.

5

Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.

Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Olschwang S, et al. Among authors: richard s. Hum Mutat. 1998;12(6):424-30. doi: 10.1002/(SICI)1098-1004(1998)12:6<424::AID-HUMU9>3.0.CO;2-H. Hum Mutat. 1998. PMID: 9829912

6

Third International Meeting on von Hippel-Lindau disease.

Zbar B, Kaelin W, Maher E, Richard S. Zbar B, et al. Among authors: richard s. Cancer Res. 1999 May 1;59(9):2251-3. Cancer Res. 1999. PMID: 10232616

7

Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions.

Gallou C, Chauveau D, Richard S, Joly D, Giraud S, Olschwang S, Martin N, Saquet C, Chrétien Y, Méjean A, Correas JM, Benoît G, Colombeau P, Grünfeld JP, Junien C, Béroud C. Gallou C, et al. Among authors: richard s. Hum Mutat. 2004 Sep;24(3):215-24. doi: 10.1002/humu.20082. Hum Mutat. 2004. PMID: 15300849

8

Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN.

Woodward ER, Ricketts C, Killick P, Gad S, Morris MR, Kavalier F, Hodgson SV, Giraud S, Bressac-de Paillerets B, Chapman C, Escudier B, Latif F, Richard S, Maher ER. Woodward ER, et al. Among authors: richard s. Clin Cancer Res. 2008 Sep 15;14(18):5925-30. doi: 10.1158/1078-0432.CCR-08-0608. Clin Cancer Res. 2008. PMID: 18794106

9

A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.

Lim DH, Rehal PK, Nahorski MS, Macdonald F, Claessens T, Van Geel M, Gijezen L, Gille JJ, Giraud S, Richard S, van Steensel M, Menko FH, Maher ER. Lim DH, et al. Among authors: richard s. Hum Mutat. 2010 Jan;31(1):E1043-51. doi: 10.1002/humu.21130. Hum Mutat. 2010. PMID: 19802896

10

Birt-Hogg-Dubé syndrome: diagnosis and management.

Menko FH, van Steensel MA, Giraud S, Friis-Hansen L, Richard S, Ungari S, Nordenskjöld M, Hansen TV, Solly J, Maher ER; European BHD Consortium. Menko FH, et al. Among authors: richard s. Lancet Oncol. 2009 Dec;10(12):1199-206. doi: 10.1016/S1470-2045(09)70188-3. Lancet Oncol. 2009. PMID: 19959076 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,460 results

Search Page