000 01464 a2200421 4500
005 20250516234138.0
264 0 _c20160106
008 201601s 0 0 eng d
022 _a1476-5438
024 7 _a10.1038/ejhg.2014.157
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWhitworth, James
245 0 0 _aA clinical and genetic analysis of multiple primary cancer referrals to genetics services.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cMay 2015
300 _a581-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aDNA Mismatch Repair
_xgenetics
650 0 4 _aExons
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenetic Testing
650 0 4 _aGerm-Line Mutation
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aNeoplasms, Multiple Primary
_xdiagnosis
650 0 4 _aPTEN Phosphohydrolase
_xgenetics
650 0 4 _aReferral and Consultation
650 0 4 _aSequence Analysis, DNA
650 0 4 _aTumor Suppressor Protein p53
_xgenetics
700 1 _aHoffman, Jon
700 1 _aChapman, Cyril
700 1 _aOng, Kai Ren
700 1 _aLalloo, Fiona
700 1 _aEvans, D Gareth
700 1 _aMaher, Eamonn R
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 23
_gno. 5
_gp. 581-7
856 4 0 _uhttps://doi.org/10.1038/ejhg.2014.157
_zAvailable from publisher's website
999 _c24215479
_d24215479