Match tier
Listed
Presence
Current · Arkansas
Last published
2023
Sources
OpenAlex · ORCID
Refreshed
2026-08-18
Biography and Research Information
OverviewAI-generated summary
N Rowley, affiliated with the University of Arkansas for Medical Sciences, has contributed to research in human genetics. Their recent publication focuses on the unique phenotypic expression observed in an infant diagnosed with a chromosome 16p13.11 deletion. This work highlights the complex interplay between genetic variations and observable health characteristics in early development.
Metrics
- Publications: 1
Selected Publications
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Unique phenoptypic expression in an infant with chromosome 16p13.11 deletion (2023)
Collaboration Network
Top Collaborators
M Baber
1 shared publication
- Unique phenoptypic expression in an infant with chromosome 16p13.11 deletion
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