ABALI, S. Et Al. 2021. Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.9 , 1201-1205.

ABALI, S., Abali, Z. Y., Yararbas, K., & SEMİZ, S., (2021). Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.9, 1201-1205.

ABALI, SAYGIN Et Al. "Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.9, 1201-1205, 2021

ABALI, SAYGIN Et Al. "Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.9, pp.1201-1205, 2021

ABALI, S. Et Al. (2021) . "Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.9, pp.1201-1205.

@article{article, author={SAYGIN ABALI Et Al. }, title={Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2021, pages={1201-1205} }