000 01516 a2200481 4500
005 20250515203934.0
264 0 _c20101207
008 201012s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/j.1399-0004.2009.01346.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMenéndez, M
245 0 0 _aFounder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.
_h[electronic resource]
260 _bClinical genetics
_cAug 2010
300 _a186-90 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlternative Splicing
_xgenetics
650 0 4 _aColorectal Neoplasms, Hereditary Nonpolyposis
_xgenetics
650 0 4 _aExons
_xgenetics
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aFounder Effect
650 0 4 _aHaplotypes
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutS Homolog 2 Protein
_xgenetics
650 0 4 _aPedigree
650 0 4 _aSpain
700 1 _aCastellví-Bel, S
700 1 _aPineda, M
700 1 _ade Cid, R
700 1 _aMuñoz, J
700 1 _aGonzález, S
700 1 _aTeulé, A
700 1 _aBalaguer, F
700 1 _aRamón y Cajal, T
700 1 _aReñé, Josep M
700 1 _aBlanco, I
700 1 _aCastells, A
700 1 _aCapellà, G
773 0 _tClinical genetics
_gvol. 78
_gno. 2
_gp. 186-90
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.2009.01346.x
_zAvailable from publisher's website
999 _c19472429
_d19472429