Publications by authors named "Ulrich Aumann"

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Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
Guntram Borck, A Kemal Topaloglu, Eckhard Korsch, Ursula Martiné, Gabriele Wildhardt, Ulrich Aumann

J Clin Endocrinol Metab· August 2004

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Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.
Joachim Pohlenz, Alexandra Dumitrescu, Ulrich Aumann, Gerhard Koch, Ralph Melchior

J Clin Endocrinol Metab· January 2002

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