P111 - Syndrome de kallmann autosomique dominant : relation...

P111 - Syndrome de kallmann autosomique dominant : relation génotypephénotype chez douze sujets présentant une mutation de FGFR1

Chabrolle, Chr., Dodé, C., Cabrol, S., Hardelin, J.-P., Chanson, Ph., Pugeat, M., Young, J.
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Volume:
65
Year:
2004
Language:
french
DOI:
10.1016/S0003-4266(04)95822-2
File:
PDF, 53 KB
french, 2004
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