Kuehnen, P. Et Al. 2014. Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.1 .

Kuehnen, P., DEMİRCİOĞLU, S., Froehler, S., GÜRAN, T., ABALI, S., Biebermann, H., ... BEREKET, A.(2014). Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.1.

Kuehnen, Peter Et Al. "Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.1, 2014

Kuehnen, Peter Et Al. "Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.1, 2014

Kuehnen, P. Et Al. (2014) . "Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.1.

@article{article, author={Peter Kuehnen Et Al. }, title={Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis}, journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM}, year=2014}