000 01536 a2200493 4500
005 20250517193100.0
264 0 _c20190305
008 201903s 0 0 eng d
022 _a1573-7292
024 7 _a10.1007/s10689-017-0067-x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _avon Salomé, Jenny
245 0 0 _aHaplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.
_h[electronic resource]
260 _bFamilial cancer
_c10 2018
300 _a531-537 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aColorectal Neoplasms, Hereditary Nonpolyposis
_xgenetics
650 0 4 _aFemale
650 0 4 _aFinland
650 0 4 _aFounder Effect
650 0 4 _aGenetics, Population
650 0 4 _aHaplotypes
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutL Protein Homolog 1
_xgenetics
650 0 4 _aMutation, Missense
650 0 4 _aPedigree
650 0 4 _aSweden
700 1 _aLiu, Tao
700 1 _aKeihäs, Markku
700 1 _aMorak, Moni
700 1 _aHolinski-Feder, Elke
700 1 _aBerry, Ian R
700 1 _aMoilanen, Jukka S
700 1 _aBaert-Desurmont, Stéphanie
700 1 _aLindblom, Annika
700 1 _aLagerstedt-Robinson, Kristina
773 0 _tFamilial cancer
_gvol. 17
_gno. 4
_gp. 531-537
856 4 0 _uhttps://doi.org/10.1007/s10689-017-0067-x
_zAvailable from publisher's website
999 _c27935411
_d27935411