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You searched for: Author/Creator Atik, Tahir

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11. Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Issue 1 (December 2015)

12. Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort. (October 2017)

14. Renal complications of lipodystrophy: A closer look at the natural history of kidney disease. (17th May 2018)

15. The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three novel germline mutations in Turkish Population. (November 2017)