Turan, I. Et Al. 2020. 21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.4 .

Turan, I., Tastan, M., Boga, D. D., GÜRBÜZ, F., KOTAN, L. D., TULİ, A., ... YÜKSEL, B.(2020). 21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.4.

Turan, İHSAN Et Al. "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.4, 2020

Turan, İHSAN Et Al. "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.4, 2020

Turan, I. Et Al. (2020) . "21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.4.

@article{article, author={İHSAN TURAN Et Al. }, title={21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2020}