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Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.

ABSTRACT: Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.

PROVIDER: PRJNA925562 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR23136839_1.fastq.gz	Fastqsanger.gz
	SRR23136839_2.fastq.gz	Fastqsanger.gz
	SRR23136840_1.fastq.gz	Fastqsanger.gz
	SRR23136840_2.fastq.gz	Fastqsanger.gz
	SRR23136841_1.fastq.gz	Fastqsanger.gz

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Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.

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