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ENDOCRINE

2 yayın · 11 atıf

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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
2024 Siklar, Zeynep, Camtosun, Emine, Bolu, Semih +37 8
Two novel <i>CYP2R1</i> mutations in a family with vitamin D-dependent rickets type 1b
2021 Ozden, Ayse, Doneray, Hakan, Turkyilmaz, Ayberk 3