Results
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1161.
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1162.
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Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. [electronic resource] by
- Pitteloud, Nelly
- Meysing, Astrid
- Quinton, Richard
- Acierno, James S
- Dwyer, Andrew A
- Plummer, Lacey
- Fliers, Eric
- Boepple, Paul
- Hayes, Frances
- Seminara, Stephanie
- Hughes, Viriginia A
- Ma, Jinghong
- Bouloux, Pierre
- Mohammadi, Moosa
- Crowley, William F
Producer: 20061025
In:
Molecular and cellular endocrinology vol. 254-255
Availability: No items available.
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1177.
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