Response to: Milosavljevic et al. "Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature"

被引：1
|
作者：
Stevens, Blair [1 ,2 ]
Johnson, Anthony [1 ,2 ]
Rowe, Thomas [3 ]
Carter, Rebecca [1 ,2 ]
Donepudi, Roopali [1 ,2 ]
机构：
[1] UT Hlth, Dept Obstet Gynecol & Reprod Sci, McGovern Med Sch, 6410 Fannin St Suite 1217, Houston, TX 77030 USA
[2] Childrens Mem Hermann Hosp, Fetal Ctr, 6410 Fannin St Suite 1217, Houston, TX 77030 USA
[3] Maternal Fetal Med Associates South Texas, Webster, TX USA
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2017年 / 173卷 / 07期
关键词：
ABNORMAL ULTRASOUND FINDINGS; MUTATIONS; GENOTYPE; FETUSES;
D O I：
10.1002/ajmg.a.38249
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：1992 / 1993
页数：2
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