1-1 of 1
Keywords: Radio-ulnar synostosis
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

A Recurrent c.416C>T Variant in the B3GAT3 Gene in the Turkish Population: Report of Two Siblings and Expanding the Clinical Spectrum

Free
Subject Area:
Genetics
Tuğba Daşar, Abdulkerim Kolkıran, Abdullah Sezer, Ercan Bal, Esra Kılıç
Journal: Molecular Syndromology
Mol Syndromol (2024) 15 (5): 409–420.
https://doi.org/10.1159/000537869
Published Online: 16 April 2024
... from any ideas, methods, instructions or products referred to in the content or advertisements. 2024 B3GAT3 Linkeropathy Kyphoscoliosis Aortic root dilatation Radio-ulnar synostosis Established Facts B3GAT3 -related linkeropathy syndrome is a rare disorder, and clinical...
View articletitled, A Recurrent c.416C>T Variant in the B3GAT3 Gene in the Turkish Population: Report of Two Siblings and Expanding the Clinical Spectrum
Open the PDF for A Recurrent c.416C>T Variant in the B3GAT3 Gene in the Turkish Population: Report of Two Siblings and Expanding the Clinical Spectrum in another window