Demirbilek, H. Et Al. 2014. Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.12 .

Demirbilek, H., Tahir, S., Baran, R. T., Sherif, M., Shah, P., Ozbek, M. N., ... Hatipoglu, N.(2014). Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.12.

Demirbilek, HÜSEYİN Et Al. "Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.12, 2014

Demirbilek, HÜSEYİN Et Al. "Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.12, 2014

Demirbilek, H. Et Al. (2014) . "Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.12.

@article{article, author={HÜSEYİN DEMİRBİLEK Et Al. }, title={Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia}, journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM}, year=2014}