G. Borck Et Al. , "Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8, pp.4136-4141, 2004
Borck, G. Et Al. 2004. Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8 , 4136-4141.
Borck, G., Topaloglu, A., Korsch, E., Martine, U., Wildhardt, G., Onenli-Mungan, N., ... Yuksel, B.(2004). Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8, 4136-4141.
Borck, G Et Al. "Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect," JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8, 4136-4141, 2004
Borck, G Et Al. "Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8, pp.4136-4141, 2004
Borck, G. Et Al. (2004) . "Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect." JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.89, no.8, pp.4136-4141.
@article{article, author={G Borck Et Al. }, title={Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: Phenotypic variability and founder effect}, journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM}, year=2004, pages={4136-4141} }