Author:
BAILLEUL-FORESTIER ISABELLE,GROS CATHERINE,ZENATY DELPHINE,BENNACEUR SÉLIM,LEGER JULIANE,De ROUX NICOLAS
Reference32 articles.
1. Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients;Sato;J Clin Endocrinol Metab,2004
2. Kallmann syndrome;Dodé;Eur J Hum Genet,2009
3. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.;Hardelin;Sex Dev,2008
4. Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism;Pitteloud;Proc Natl Acad Sci USA,2006
5. Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1);Zenaty;Mol Cell Endocrinol,2006
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