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A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations
Vallette‐Kasic, S., Pulichino, A.‐M., Gueydan, M., Barlier, A., David, M., Malpuech, G., Deal, C., Van Vliet, G., de Vroede, M., Riepe, F., Partsch, C.‐J., Sippell, W., Berberoglu, M., Atasay, B., deVolume:
30
Language:
english
Journal:
Endocrine Research
DOI:
10.1081/erc-200044166
Date:
January, 2004
File:
PDF, 57 KB
english, 2004