4Bum J, Goodship J. Developmental genetics of the heart. Curr Opinion Genet Devel, 1996,6:322 - 326.
5Matsuoka R, Kimura M, Scambler PJ, et al. Molecular and clinical study of 183 patients with conotruncul anomaly face syndrome. Hum Genet, 1998,103 : 70 - 80.
6Yamagishi H, Garg V, Matsuoka R, et al. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.Science, 1999,283 : 1158 - 1161.
7Momma K, Kondo C, Ando M, et al. Tetralogy of Fallot with chromosome 22q 11.2 deletion. Am J Cardiol, 1995,76 : 618 - 621.
8Didier D, Ratib O, Beghetti M, et al. Morpholngic and functional evalution of congenital heart disease by magnetic resonance imaging. J Magn Reson Imaging, 1999,10:639 - 655.
9Rpche KJ, Krinsky G, Lee VS, et al. Interrupted aortic arch : diagnosis with gadolinium - enhancd 3D MRA. J Comput Assist Tomogr, 1999,23 : 197- 202.
10Hijazi ZM. Hakim F, Fadley F, et al. Transcatheler closure of single muscular ventricular septal defects using the amplatzer muscular VSD occluder. Catheter Cardiovasc Interv, 2000,49(2) : 167 - 170.
二级参考文献25
1[1]Amplaz K, Moller JH. 《Radiology of congenital heart disease》. St. Louis: MO. Mosby, 1993:243~244