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	1.	Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene. [electronic resource] by Pitteloud, Nelly Acierno, James S Meysing, Astrid U Dwyer, Andrew A Hayes, Frances J Crowley, William F Producer: 20050412 In: The Journal of clinical endocrinology and metabolism vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	GNRHR mutations in a woman with idiopathic hypogonadotropic hypogonadism highlight the differential sensitivity of luteinizing hormone and follicle-stimulating hormone to gonadotropin-releasing hormone. [electronic resource] by Meysing, Astrid U Kanasaki, Haruhiko Bedecarrats, Gregoy Y Acierno, James S Conn, P Michael Martin, Kathryn A Seminara, Stephanie B Hall, Janet E Crowley, William F Kaiser, Ursula B Producer: 20040810 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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