Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
This study introduced whole-exome sequencing (WES) in prenatal diagnosis of fetal bowel dilatation to improve the detection outcome when karyotype analysis and copy number variation sequencing (CNV-seq) were uninformative in detecting pathogenic variants. The work reviewed 28 cases diagnosed with fe...
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| Principais autores: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
De Gruyter
2023-05-01
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| coleção: | Open Life Sciences |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1515/biol-2022-0598 |
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