000 01305 a2200373 4500
005 20250515174235.0
264 0 _c20110923
008 201109s 0 0 eng d
022 _a1874-1754
024 7 _a10.1016/j.ijcard.2009.05.030
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWang, Binbin
245 0 0 _aForkhead box H1 (FOXH1) sequence variants in ventricular septal defect.
_h[electronic resource]
260 _bInternational journal of cardiology
_cNov 2010
300 _a83-5 p.
_bdigital
500 _aPublication Type: Comparative Study; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Sequence
650 0 4 _aAsian People
_xgenetics
650 0 4 _aCohort Studies
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aGenetic Variation
_xgenetics
650 0 4 _aHeart Septal Defects, Ventricular
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
_xgenetics
700 1 _aYan, Jinting
700 1 _aMi, Rui
700 1 _aZhou, Shiyi
700 1 _aXie, Xiaodong
700 1 _aWang, Jing
700 1 _aMa, Xu
773 0 _tInternational journal of cardiology
_gvol. 145
_gno. 1
_gp. 83-5
856 4 0 _uhttps://doi.org/10.1016/j.ijcard.2009.05.030
_zAvailable from publisher's website
999 _c18944335
_d18944335