Eren, E. Et Al. 2023. Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.. Journal of clinical research in pediatric endocrinology , vol.15 , 97-102.

Eren, E., Tezcan Unlu, H., Ceylaner, S., & Tarim, Ö. F., (2023). Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.. Journal of clinical research in pediatric endocrinology , vol.15, 97-102.

Eren, ERDAL Et Al. "Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.," Journal of clinical research in pediatric endocrinology , vol.15, 97-102, 2023

Eren, ERDAL Et Al. "Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.." Journal of clinical research in pediatric endocrinology , vol.15, pp.97-102, 2023

Eren, E. Et Al. (2023) . "Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.." Journal of clinical research in pediatric endocrinology , vol.15, pp.97-102.

@article{article, author={ERDAL EREN Et Al. }, title={Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2.}, journal={Journal of clinical research in pediatric endocrinology}, year=2023, pages={97-102} }