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De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening.
Prenatal Diagnosis ( IF 2.7 ) Pub Date : 2020-09-09 , DOI: 10.1002/pd.5798
Chidinma Nwakalor 1 , Sara Said-Delgado 2 , Shifra Krinshpun 3 , Milen Velinov 4, 5
Affiliation  



中文翻译:

通过非侵入性无细胞胎儿 DNA 筛查确定与 Costello 综合征相关的从头 HRAS 基因突变。

更新日期:2020-07-18
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