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The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. [electronic resource] by
- Oliveira, L M
- Seminara, S B
- Beranova, M
- Hayes, F J
- Valkenburgh, S B
- Schipani, E
- Costa, E M
- Latronico, A C
- Crowley, W F
- Vallejo, M
Producer: 20010503
In:
The Journal of clinical endocrinology and metabolism vol. 86
Availability: No items available.
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13.
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Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism. [electronic resource] by
- Beranova, M
- Oliveira, L M
- Bédécarrats, G Y
- Schipani, E
- Vallejo, M
- Ammini, A C
- Quintos, J B
- Hall, J E
- Martin, K A
- Hayes, F J
- Pitteloud, N
- Kaiser, U B
- Crowley, W F
- Seminara, S B
Producer: 20010503
In:
The Journal of clinical endocrinology and metabolism vol. 86
Availability: No items available.
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