טוען...
Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing
A prospective analysis investigating the associations between pathogenic copy number variations (pCNVs) and ultrasound soft markers (USMs) in fetuses and evaluating the clinical value of copy number variation sequencing (CNV-seq) in such pregnancy studies was carried out. 3,398 unrelated Chinese wom...
שמור ב:
| הוצא לאור ב: | Sci Rep |
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| Main Authors: | , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group UK
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5970175/ https://ncbi.nlm.nih.gov/pubmed/29802277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-26555-6 |
| תגים: |
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