Page 208 - CHD
P. 208

参考文献





              [8]Antonarakis SE,Lyle R,Dermitzakis ET,et al. Chromosome 21 and clown syndrome:from genomics to


              pathophysiology [J]. Nat Rev Genet,2004,5(10)725-738.


              [9]Font SJ, Robbins JM , Bird TM , el al. Congenita) malfonnations among liveboni infants with trisomies 18 and 13 [J].


              Am J Med Genet A ,2006 ,140(16) :1749-1756.



              [10]J Zaidi S, Bnieckner M. Genetics and genomics of congenital heart disease[J].Circ Res,2017,120(6) :923-940.


              [11]Bondy CA. I'urner syndrome 2008 [J]. Horni Res,2009 ,71 (Suppl 1):S52-56.


              [12]Pinsker JE. Clinical review:Turner syndrome: updating the paradigmn ofclinical care[J]. J Clin Endocrinol Metab,


              2012,97 ( 6 ):e994-1003.


              [13]Koczkowska M , Wierzba J , S migiel R, et al. Genomic findings in patients with clinical suspicion of 22q11.2


              deletion syndrome [J]. J Appl Genet,2017,58(1):93-98. DOI:10. 1007/s13353-016-0366-1.


              [14]秦玉峰,解春红,杨建滨,等.22q11微缺失综合征与先天性心脏病的关系[J].中华心血管病杂


              志,2011,39(7):631-635. D0I:10.3760/cma. j. issn. 0253-3758. 2011.07.007.
   203   204   205   206   207   208   209   210   211   212   213