The NR2F1-related 5q14.3–q21.1 deletion causing periventricular heterotopia with cerebral visual impairment: The NR2F1-related 5q14.3–q21.1 deletion causing periventricular heterotopia with cerebral visual impairment (dataset)

Helen St Clair Tracy (Creator)
Andrew Blaikie (Creator)

Dataset

Date made available	2026
Publisher	NCBI GenBank

Contact

[email protected]

Access Dataset

Identifiers GRCh38/hg38 5q14.3-21.2(chr5:90079852-103658165)x1

1 Article

The NR2F1-related 5q14.3–q21.1 deletion causing periventricular heterotopia with cerebral visual impairment: a longitudinal case report and genotype–phenotype analysis
St Clair Tracy, H., Dutton, G. N., Hall, H. N. & Blaikie, A., 7 May 2026, (E-pub ahead of print) In: Frontiers in Genetics. 17, 1793726.
Research output: Contribution to journal › Article › peer-review

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