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Compound heterozygous and homozygous mutations of the TSH beta gene as a cause of congenital central hypothyroidism in Europe
Karges, B et al. (2004)
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UKU. Klinik für Innere Medizin I (1)
UKU. Klinik für Kinder- und Jugendmedizin (1)Person
Andler, W (1)
Castro-Correia, C (1)
Debatin, Klaus-Michael (1)
... View MoreResource typeWissenschaftlicher Artikel (1)Issue date2004 (1)University Bibliography
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