No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome

Pia Vahteristo, Taru A. Koski, Laura Naatsaari, Maija Kiuru, Auli Karhu, Riitta Herva, Satu-Leena Sallinen, Outi Vierimaa, Erik Bjorck, Stephane Richard, Betty Gardie, Didier Bessis, Emmanuel Van Glabeke, Ignacio Blanco, Richard Houlston, Leigha Senter, Marja Hietala, Kristiina Aittomaki, Lauri A. Aaltonen, Virpi LaunonenRainer Lehtonen

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Originalspråkengelska
TidskriftFamilial Cancer
Volym9
Sidor (från-till)245-251
Antal sidor7
ISSN1389-9600
DOI
StatusPublicerad - 2010
MoE-publikationstypA1 Tidskriftsartikel-refererad

Citera det här

Vahteristo, Pia ; Koski, Taru A. ; Naatsaari, Laura ; Kiuru, Maija ; Karhu, Auli ; Herva, Riitta ; Sallinen, Satu-Leena ; Vierimaa, Outi ; Bjorck, Erik ; Richard, Stephane ; Gardie, Betty ; Bessis, Didier ; Van Glabeke, Emmanuel ; Blanco, Ignacio ; Houlston, Richard ; Senter, Leigha ; Hietala, Marja ; Aittomaki, Kristiina ; Aaltonen, Lauri A. ; Launonen, Virpi ; Lehtonen, Rainer. / No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome. I: Familial Cancer. 2010 ; Vol. 9. s. 245-251.
@article{0337f2c3d93346788ccb6323a76ab1a0,
title = "No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome",
keywords = "Fumarate hydratase, Genetic testing, HLRCC, Modifier, Renal cell cancer, FUMARATE HYDRATASE MUTATIONS, HEREDITARY LEIOMYOMATOSIS, UTERINE LEIOMYOMATOSIS, CUTANEOUS LEIOMYOMATOSIS, MISSENSE MUTATIONS, CLINICAL-FEATURES, TUMOR SYNDROME, FH, PARAGANGLIOMA, DEFICIENCY",
author = "Pia Vahteristo and Koski, {Taru A.} and Laura Naatsaari and Maija Kiuru and Auli Karhu and Riitta Herva and Satu-Leena Sallinen and Outi Vierimaa and Erik Bjorck and Stephane Richard and Betty Gardie and Didier Bessis and {Van Glabeke}, Emmanuel and Ignacio Blanco and Richard Houlston and Leigha Senter and Marja Hietala and Kristiina Aittomaki and Aaltonen, {Lauri A.} and Virpi Launonen and Rainer Lehtonen",
year = "2010",
doi = "10.1007/s10689-009-9312-2",
language = "English",
volume = "9",
pages = "245--251",
journal = "Familial Cancer",
issn = "1389-9600",
publisher = "Springer",

}

Vahteristo, P, Koski, TA, Naatsaari, L, Kiuru, M, Karhu, A, Herva, R, Sallinen, S-L, Vierimaa, O, Bjorck, E, Richard, S, Gardie, B, Bessis, D, Van Glabeke, E, Blanco, I, Houlston, R, Senter, L, Hietala, M, Aittomaki, K, Aaltonen, LA, Launonen, V & Lehtonen, R 2010, 'No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome', Familial Cancer, vol. 9, s. 245-251. https://doi.org/10.1007/s10689-009-9312-2

No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome. / Vahteristo, Pia; Koski, Taru A.; Naatsaari, Laura; Kiuru, Maija; Karhu, Auli; Herva, Riitta; Sallinen, Satu-Leena; Vierimaa, Outi; Bjorck, Erik; Richard, Stephane; Gardie, Betty; Bessis, Didier; Van Glabeke, Emmanuel; Blanco, Ignacio; Houlston, Richard; Senter, Leigha; Hietala, Marja; Aittomaki, Kristiina; Aaltonen, Lauri A.; Launonen, Virpi; Lehtonen, Rainer.

I: Familial Cancer, Vol. 9, 2010, s. 245-251.

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

TY - JOUR

T1 - No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome

AU - Vahteristo, Pia

AU - Koski, Taru A.

AU - Naatsaari, Laura

AU - Kiuru, Maija

AU - Karhu, Auli

AU - Herva, Riitta

AU - Sallinen, Satu-Leena

AU - Vierimaa, Outi

AU - Bjorck, Erik

AU - Richard, Stephane

AU - Gardie, Betty

AU - Bessis, Didier

AU - Van Glabeke, Emmanuel

AU - Blanco, Ignacio

AU - Houlston, Richard

AU - Senter, Leigha

AU - Hietala, Marja

AU - Aittomaki, Kristiina

AU - Aaltonen, Lauri A.

AU - Launonen, Virpi

AU - Lehtonen, Rainer

PY - 2010

Y1 - 2010

KW - Fumarate hydratase

KW - Genetic testing

KW - HLRCC

KW - Modifier

KW - Renal cell cancer

KW - FUMARATE HYDRATASE MUTATIONS

KW - HEREDITARY LEIOMYOMATOSIS

KW - UTERINE LEIOMYOMATOSIS

KW - CUTANEOUS LEIOMYOMATOSIS

KW - MISSENSE MUTATIONS

KW - CLINICAL-FEATURES

KW - TUMOR SYNDROME

KW - FH

KW - PARAGANGLIOMA

KW - DEFICIENCY

U2 - 10.1007/s10689-009-9312-2

DO - 10.1007/s10689-009-9312-2

M3 - Article

VL - 9

SP - 245

EP - 251

JO - Familial Cancer

JF - Familial Cancer

SN - 1389-9600

ER -