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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31.
Funct Integr Genomics. 2022.
PMID: 35098403
A case of familial recurrent 17q12 microdeletion syndrome presenting with severe diabetic ketoacidosis.
Aydın C, Kıral E, Susam E, Tufan AK, Yarar C, Çetin N, Kocagil S, Kırel B.
Aydın C, et al. Among authors: susam e.
Turk J Pediatr. 2022;64(3):558-565. doi: 10.24953/turkjped.2021.1613.
Turk J Pediatr. 2022.
PMID: 35899569
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