Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases

被引:0
作者
Zhang, Yan [1 ]
Ding, Can [2 ]
Chen, Yiwei [3 ]
Wu, Meng [4 ,5 ]
Luo, Min [6 ]
机构
[1] Guangdong Women & Children Hosp, Ctr Med Genet, Guangzhou, Peoples R China
[2] Univ Med Marburg, Campus Fulda, Fulda, Germany
[3] Wonder Sir, Shanghai, Peoples R China
[4] Shandong First Med Univ, Shandong Canc Hosp & Inst, Shandong Prov Key Lab Radiat Oncol, Jinan, Peoples R China
[5] Shandong Acad Med Sci, Jinan, Peoples R China
[6] Natl Univ Singapore, Dept Biol Sci, Singapore, Singapore
关键词
exome sequencing; phenotype [mesh; prenetal diagnosis; fetal abnormalities; rare disease (RD);
D O I
10.3389/fgene.2023.1205726
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
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页数:2
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