Publications

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Filters: Author is Uludağ Alkaya, Dilek  [Clear All Filters]
2021
Alkaya, D. Uludağ, Akpınar, E., Bilguvar, K. & Tuysuz, B. Resolution of sclerotic lesions of dysosteosclerosis due to biallelic SLC29A3 variant in a Turkish girl. Am J Med Genet A (2021). doi:10.1002/ajmg.a.62198
2018
Yilmaz, S. et al. Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. Mol Genet Genomic Med 6, 230-248 (2018).