000 01233 a2200349 4500
005 20250515043031.0
264 0 _c20070306
008 200703s 0 0 eng d
022 _a0006-4971
024 7 _a10.1182/blood-2006-07-037853
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSmith, Alexandra G
245 0 0 _aA common genetic variant in XPD associates with risk of 5q- and 7q-deleted acute myeloid leukemia.
_h[electronic resource]
260 _bBlood
_cFeb 2007
300 _a1233-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAcute Disease
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 5
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenetic Variation
650 0 4 _aGlutamine
650 0 4 _aHumans
650 0 4 _aLeukemia, Myeloid
_xepidemiology
650 0 4 _aPrognosis
650 0 4 _aXeroderma Pigmentosum Group D Protein
_xgenetics
700 1 _aWorrillow, Lisa J
700 1 _aAllan, James M
773 0 _tBlood
_gvol. 109
_gno. 3
_gp. 1233-6
856 4 0 _uhttps://doi.org/10.1182/blood-2006-07-037853
_zAvailable from publisher's website
999 _c16600526
_d16600526