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Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study
Background: Prenatal diagnosis of fetal short long bones (SLBs) was reported to be associated with skeletal dysplasias, chromosomal abnormalities, and genetic syndromes. This study aims to identify the genetic causes for fetal short long bones, and retrospectively evaluate the additional diagnostic...
| Những tác giả chính: | , , , , , , , , , |
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| Định dạng: | Online Bài viết Texto |
| Ngôn ngữ: | English |
| Được phát hành: |
Frontiers Media S.A.
2023
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| Những chủ đề: | |
| Truy cập trực tuyến: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010437/ https://www.ncbi.nlm.nih.gov/pubmed/36923788 http://dx.doi.org/10.3389/fgene.2023.1032346 |