000 01752 a2200529 4500
005 20250516025736.0
264 0 _c20120125
008 201201s 0 0 eng d
022 _a1471-2261
024 7 _a10.1186/1471-2261-11-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aScheffold, Thomas
245 0 0 _aSix sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.
_h[electronic resource]
260 _bBMC cardiovascular disorders
_cMar 2011
300 _a9 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article; Multicenter Study
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChromosomes, Human, Pair 9
_xgenetics
650 0 4 _aGenetic Variation
_xgenetics
650 0 4 _aGenome-Wide Association Study
_xmethods
650 0 4 _aHaplotypes
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMyocardial Infarction
_xdiagnosis
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aRegistries
650 0 4 _aYoung Adult
700 1 _aKullmann, Silke
700 1 _aHuge, Andreas
700 1 _aBinner, Priska
700 1 _aOchs, Hermann R
700 1 _aSchöls, Wolfgang
700 1 _aThale, Joachim
700 1 _aMotz, Wolfgang
700 1 _aHegge, Franz Josef
700 1 _aStellbrink, Christoph
700 1 _aDorsel, Thomas
700 1 _aGülker, Hartmut
700 1 _aHeuer, Hubertus
700 1 _aDinh, Wilfried
700 1 _aStoll, Monika
700 1 _aHaltern, Georg
773 0 _tBMC cardiovascular disorders
_gvol. 11
_gp. 9
856 4 0 _uhttps://doi.org/10.1186/1471-2261-11-9
_zAvailable from publisher's website
999 _c20657837
_d20657837