HORMONOGENIC DEFECTS IN INHERITED THYROID DISEASES
- 2 Anni 1999/2001
- 103.291€ Totale Fondi
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Pubblicazioni Scientifiche
- AMERICAN JOURNAL OF HUMAN GENETICS
Mapping a dominant form of multinodular goiter to chromosome Xp22
- THYROID
Genetics of specific phenotypes of congenital hypothyroidism: A population-based approach
