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, WD repeat domain 72
National Institutes of Health
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Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool.
Corpus ID: 205026285
Amelogenesis imperfecta (AI) is a clinically and genetically heterogeneous disorder of tooth development which is due to aberrant…
Spatiotemporal expression profile of a putative β propeller WDR72 in laying hens
Molecular Biology Reports
Corpus ID: 13196253
The purpose of this study is to characterize the expression profile of a novel gene WDR72 in laying hens. Sixty-week old Hy-line…
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)
BMC Medical Genetics
Corpus ID: 1781275
BackgroundChronic hyperglycemia confers increased risk for long-term diabetes-associated complications and repeated hemoglobin…
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