Çiftci, N. Et Al. 2022. 46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.. Journal of clinical research in pediatric endocrinology , vol.14 , 233-238.

Çiftci, N., Kayaş, L., Çamtosun, E., & Akıncı, A., (2022). 46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.. Journal of clinical research in pediatric endocrinology , vol.14, 233-238.

Çiftci, Nurdan Et Al. "46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.," Journal of clinical research in pediatric endocrinology , vol.14, 233-238, 2022

Çiftci, Nurdan Et Al. "46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.." Journal of clinical research in pediatric endocrinology , vol.14, pp.233-238, 2022

Çiftci, N. Et Al. (2022) . "46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.." Journal of clinical research in pediatric endocrinology , vol.14, pp.233-238.

@article{article, author={Nurdan Çiftci Et Al. }, title={46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.}, journal={Journal of clinical research in pediatric endocrinology}, year=2022, pages={233-238} }