S. Acar Et Al. , "Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7," JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4, pp.773-786, 2022
Acar, S. Et Al. 2022. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4 , 773-786.
Acar, S., Gursoy, S., Arslan, G., Nalbantoglu, O., Hazan, F., Koprulu, O., ... Ozkaya, B.(2022). Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4, 773-786.
Acar, S. Et Al. "Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7," JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4, 773-786, 2022
Acar, S. Et Al. "Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7." JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4, pp.773-786, 2022
Acar, S. Et Al. (2022) . "Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7." JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.45, no.4, pp.773-786.
@article{article, author={S. Acar Et Al. }, title={Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7}, journal={JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION}, year=2022, pages={773-786} }