![](/img/cover-not-exists.png)
Four New Cases of Congenital Secondary Hypothyroidism due to a Splice Site Mutation in the Thyrotropin-β Gene: Phenotypic Variability and Founder Effect
Borck, Guntram, Topaloglu, A. Kemal, Korsch, Eckhard, Martiné, Ursula, Wildhardt, Gabriele, Onenli-Mungan, Neslihan, Yuksel, Bilgin, Aumann, Ulrich, Koch, Gerhard, Ozer, Guler, Pfäffle, Roland, ScherbVolume:
89
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jc.2004-0494
Date:
August, 2004
File:
PDF, 177 KB
english, 2004