Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia
Skeletal dysplasia is a complex group of bone and cartilage disorders with strong clinical and genetic heterogeneity. Several types have prenatal phenotypes, and it is difficult to make a molecular diagnosis rapidly. In this study, the genetic cause of 16 Chinese fetuses with skeletal dysplasia were...
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| Principais autores: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Media S.A.
2021-03-01
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| סדרה: | Frontiers in Genetics |
| נושאים: | |
| גישה מקוונת: | https://www.frontiersin.org/articles/10.3389/fgene.2021.599863/full |
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