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Updated: Apr 16, 2026

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I
Esra Kilic1, Gökhan Yigit, Gülen Eda Utine
1Faculty of Medicine, Division of Pediatric Genetics, Hacettepe University, Ankara, Turkey.
American Journal of Medical Genetics. Part A
|March 5, 2015
Abstract
No abstract available in PubMed .
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