F. ATALAR Et Al. , "CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children," 43rd Annual Meeting European Society for Paediatric Endocrinology , Switzerland, pp.109, 0
ATALAR, F. Et Al. CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children. 43rd Annual Meeting European Society for Paediatric Endocrinology , (Switzerland), 109.
ATALAR, F., WOLLNIK, B., DARENDELILER, F., BAŞ, F., GÜNÖZ, H., KAYSERILI, H., ... SAKA, N. CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children . 43rd Annual Meeting European Society for Paediatric Endocrinology (pp.109). , Switzerland
ATALAR, Fatmahan Et Al. "CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children," 43rd Annual Meeting European Society for Paediatric Endocrinology, Switzerland,
ATALAR, Fatmahan Et Al. "CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children." 43rd Annual Meeting European Society for Paediatric Endocrinology , Switzerland, pp.109
ATALAR, F. Et Al. . "CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children." 43rd Annual Meeting European Society for Paediatric Endocrinology , Switzerland, p.109.
@conferencepaper{conferencepaper, author={Fatmahan ATALAR Et Al. }, title={CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children}, congress name={43rd Annual Meeting European Society for Paediatric Endocrinology}, city={}, country={Switzerland}, year={0}, pages={109} }