# Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/whole-exome-sequencing-as-a-diagnostic-adjunct-to-clinical-testing-in-fetuses/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Fang Fu,R. Li,Y. Li,Zhiqiang Nie,T. Lei,Dan Wang,Xiaohong Yang,Jin Han,Min Pan,Zhen Li,Yu‐Che Ou,Junjie Li,Fatao Li,Jing Xu,Duan Li,Can Liao |
| Citations | 171 |
| DOI | 10.1002/uog.18915 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/uog.18915 |
| OpenAlex ID | https://openalex.org/W2797817786 |
| PMID | 28976722 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Zhen Li](https://scholariq.org/researchers/zhen-li-2/)

## Paper primary topic

- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)

## Paper topics

- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.