Studies
The Molecular Basis of Inherited Reproductive Disorders
The Molecular Basis of Inherited Reproductive Disorders
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Overview
Selected Publications (3)
The GPR54 gene as a regulator of puberty.
S. Seminara, S. Messager, E. Chatzidaki, et al.. (2004). The New England journal of medicine. Cited 1,257 times.
https://doi.org/10.1097/00006254-200405000-00020
TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
A. Topaloğlu, F. Reimann, M. Guclu, et al.. (2009). Nature Genetics. Cited 878 times.
https://doi.org/10.1038/ng.306
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
C. Dodé, J. Levilliers, J. Dupont, et al.. (2003). Nature Genetics. Cited 791 times.
https://doi.org/10.1038/ng1122
