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Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers
BACKGROUND: Some ultrasonic soft markers can be found during ultrasound examination. However, the etiology of the fetuses with ultrasonic soft markers is still unknown. This study aimed to evaluate the genetic etiology and clinical value of chromosomal abnormalities and copy number variations (CNVs)...
Tallennettuna:
| Julkaisussa: | BMC Med Genomics |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7802188/ https://ncbi.nlm.nih.gov/pubmed/33435955 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-021-00870-w |
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