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Mutations in fibroblast growth factor receptor 1 cause Kall..:
Pitteloud, Nelly
;
Meysing, Astrid
;
Quinton, Richard
...
Molecular and Cellular Endocrinology. 254-255 (2006) - p. 60-69 , 2006
Link:
https://doi.org/10.1016/j.mce.2006.04.021
RT Journal T1
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.mce.2006.04.021&Exemplar=1&LAN=DE A1 Pitteloud, Nelly A1 Meysing, Astrid A1 Quinton, Richard A1 Acierno Jr., James S. A1 Dwyer, Andrew A. A1 Plummer, Lacey A1 Fliers, Eric A1 Boepple, Paul A1 Hayes, Frances A1 Seminara, Stephanie A1 Hughes, Viriginia A. A1 Ma, Jinghong A1 Bouloux, Pierre A1 Mohammadi, Moosa A1 Crowley Jr., William F. PB Elsevier BV YR 2006 SN 0303-7207 JF Molecular and Cellular Endocrinology VO 254-255 SP 60 OP 69 LK http://dx.doi.org/https://doi.org/10.1016/j.mce.2006.04.021 DO https://doi.org/10.1016/j.mce.2006.04.021 SF ELIB - SuUB Bremen
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