Genetic insights into human isolated gonadotropin deficiency

Author:

Trarbach Ericka Barbosa,Silveira Leticia Gontijo,Latronico Ana Claudia

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference99 articles.

1. Palmert MR, Boepple PA (2001) Variation in the timing of puberty: clinical spectrum and genetic investigation. J Clin Endocrinol Metab 86:2364–2368

2. Seminara SB, Hayes FJ, Crowley WF Jr (1998) Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann’s syndrome): pathophysiological and genetic considerations. Endocr Rev 19:521–539

3. Pawlowitzki IH, Diekstall P, Schadel A, Miny P (1987) Estimating frequency of Kallmann syndrome among hypogonadic and among anosmic patients. Am J Med Genet 26:473–479

4. Oliveira LM, Seminara SB, Beranova M, Hayes FJ, Valkenburgh SB, Schipani E, Costa EM, Latronico AC, Crowley WF Jr, Vallejo M (2001) The importance of autosomal genes in Kallmann syndrome: genotype–phenotype correlations and neuroendocrine characteristics. J Clin Endocrinol Metab 86:1532–1538

5. Georgopoulos N, Pralong F, Seidman C, Seidman J, Crowley WJ, Vallejo M (1997) Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. J Clin Endocrinol Metab 82:213–217

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