DOI:
10.1055/s-00000017
Experimental and Clinical Endocrinology & Diabetes
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References
Zenaty D, Bretones P, Lambe C. et al.
Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth
factor receptor 1 (FGFR1).
Mol Cell Endocrinol 2006;
254-255: 78-83
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