000 01381 a2200397 4500
005 20250517171307.0
264 0 _c20180201
008 201802s 0 0 eng d
022 _a1476-5438
024 7 _a10.1038/ejhg.2017.132
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSeppälä, Toni T
245 0 0 _aUptake of genetic testing by the children of Lynch syndrome variant carriers across three generations.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_c11 2017
300 _a1237-1245 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aColorectal Neoplasms, Hereditary Nonpolyposis
_xdiagnosis
650 0 4 _aDNA-Binding Proteins
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Testing
_xstatistics & numerical data
650 0 4 _aHeterozygote
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
650 0 4 _aPedigree
700 1 _aPylvänäinen, Kirsi
700 1 _aMecklin, Jukka-Pekka
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 25
_gno. 11
_gp. 1237-1245
856 4 0 _uhttps://doi.org/10.1038/ejhg.2017.132
_zAvailable from publisher's website
999 _c27489575
_d27489575