E. EREN Et Al. , "Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, pp.218-223, 2016
EREN, E. Et Al. 2016. Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2 , 218-223.
EREN, E., EDGÜNLÜ, T., Asut, E., & Celik, S. K., (2016). Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, 218-223.
EREN, ERDAL Et Al. "Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, 218-223, 2016
EREN, ERDAL Et Al. "Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, pp.218-223, 2016
EREN, E. Et Al. (2016) . "Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, pp.218-223.
@article{article, author={ERDAL EREN Et Al. }, title={Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2016, pages={218-223} }