C. R. Hughes Et Al. , "Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7, pp.3497-3501, 2010
Hughes, C. R. Et Al. 2010. Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7 , 3497-3501.
Hughes, C. R., Chung, T. T., Habeb, A. M., Kelestimur, F., Clark, A. J. L., & Metherell, L. A., (2010). Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7, 3497-3501.
Hughes, Hasan Et Al. "Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7, 3497-3501, 2010
Hughes, Hasan F. Et Al. "Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7, pp.3497-3501, 2010
Hughes, C. R. Et Al. (2010) . "Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.95, no.7, pp.3497-3501.
@article{article, author={Hasan Fahrettin KELEŞTEMUR Et Al. }, title={Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2}, journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM}, year=2010, pages={3497-3501} }