The implementation of Whole Exome Sequencing in the molecular diagnosis of fetal structural anomalies: the experience of a referral Italian hospital

被引：0
|
作者：
Zampieri, Stefania [1 ]
Feresin, Agnese [2 ]
Morgan, Anna [1 ]
Paccagnella, Elisa [1 ]
Rubinato, Elisa [1 ]
Mazza, Daniela [1 ]
Perino, Federica [2 ]
Samarin, Anna [2 ]
Stampalija, Tamara [2 ,3 ]
Pinamonti, Maurizio [4 ,5 ]
Turchetto, Giovanni [1 ]
Bussani, Rossana [2 ,4 ,5 ]
Spedicati, Beatrice [1 ,2 ]
Murru, Flora Maria [2 ,6 ]
Girotto, Giorgia [1 ,2 ]
机构：
[1] IRCCS Burlo Garofolo, SC Genet Med, Trieste, Italy
[2] Univ Trieste, Dept Med Surg & Hlth Sci, Trieste, Italy
[3] IRCCS Burlo Garofolo, Fetal Med & Prenatal Diag Unit, Trieste, Italy
[4] Azienda Sanitaria Univ Giuliano Isontina, Trieste, Italy
[5] Univ Trieste, Dept Pathol, Trieste, Italy
[6] IRCCS Burlo Garofolo, Paediat Radiol, Trieste, Italy
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P03.028.D
引用
收藏
页码：1314 / 1315
页数：2
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