Correspondence regarding genetic assessment following increased nuchal translucency and normal karyotype

被引：0
|
作者：
Briere, Lauren C. [1 ]
Roberts, Amy E. [2 ]
Joshi, Victoria [3 ]
机构：
[1] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] Childrens Hosp, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
来源：
PRENATAL DIAGNOSIS | 2012年 / 32卷 / 06期
关键词：
NOONAN-SYNDROME; SOS1; MUTATIONS;
D O I：
10.1002/pd.2920
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：607 / 608
页数：2
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