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Mutations in fibroblast growth factor receptor 1 cause both..:
Pitteloud, Nelly
;
Acierno Jr., James S.
;
Meysing, Astrid
...
Proceedings of the National Academy of Sciences. 103 (2006) 16 - p. 6281-6286 , 2006
Link:
https://doi.org/10.1073/pnas.0600962103
RT Journal T1 <Title>Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1073_pnas.0600962103&Exemplar=1&LAN=DE A1 Pitteloud, Nelly A1 Acierno Jr., James S. A1 Meysing, Astrid A1 Eliseenkova, Anna V. A1 Ma, Jinghong A1 Ibrahimi, Omar A. A1 Metzger, Daniel L. A1 Hayes, Frances J. A1 Dwyer, Andrew A. A1 Hughes, Virginia A. A1 Yialamas, Maria A1 Hall, Janet E. A1 Grant, Ellen A1 Mohammadi, Moosa A1 Crowley Jr., William F. PB Proceedings of the National Academy of Sciences YR 2006 SN 0027-8424 SN 1091-6490 JF Proceedings of the National Academy of Sciences VO 103 IS 16 SP 6281 OP 6286 LK http://dx.doi.org/https://doi.org/10.1073/pnas.0600962103 DO https://doi.org/10.1073/pnas.0600962103 SF ELIB - SuUB Bremen
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