P200: A novel 13q31.3q32.3 deletion identified on follow up of an inconclusive prenatal cell-Free DNA screening for trisomy 13

Berger, S., Mito, Y., & Mehta, L. (2024). P200: A novel 13q31.3q32.3 deletion identified on follow up of an inconclusive prenatal cell-Free DNA screening for trisomy 13. Genetics in Medicine Open, 2, 101097. https://doi.org/10.1016/j.gimo.2024.101097
Authors:
Sara Berger
Yoshiko Mito
Lakshmi Mehta
Affiliated Authors:
Sara Berger
Lakshmi Mehta
Columbia Affiliation:
Subjects:
Genomic Rearrangements and Copy Number Variations (OpenAlex Topic)
RNA Methylation and Modification in Gene Expression (OpenAlex Topic)
Glycosylation in Health and Disease (OpenAlex Topic)
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Publication Type:
Article
Unique ID:
10.1016/j.gimo.2024.101097
DOI:
10.1016/j.gimo.2024.101097
Journal:
Genetics in Medicine Open
Publication Date:
Data Source:
OpenAlex
Source Link:
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