S. Turan Et Al. , "An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).," The Journal of clinical endocrinology and metabolism , vol.97, no.5, 2012
Turan, S. Et Al. 2012. An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).. The Journal of clinical endocrinology and metabolism , vol.97, no.5 .
Turan, S., Hughes, C., Atay, Z., GÜRAN, T., Haliloglu, B., Clark, A. J. L., ... BEREKET, A.(2012). An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).. The Journal of clinical endocrinology and metabolism , vol.97, no.5.
Turan, SERAP Et Al. "An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).," The Journal of clinical endocrinology and metabolism , vol.97, no.5, 2012
Turan, SERAP Et Al. "An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).." The Journal of clinical endocrinology and metabolism , vol.97, no.5, 2012
Turan, S. Et Al. (2012) . "An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).." The Journal of clinical endocrinology and metabolism , vol.97, no.5.
@article{article, author={SERAP DEMİRCİOĞLU Et Al. }, title={An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).}, journal={The Journal of clinical endocrinology and metabolism}, year=2012}