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	1.	Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred. [electronic resource] by Brunner, Elisa Baima, Jader Vieira, Teresa C Vieira, José G H Abucham, Julio Producer: 20030825 In: Clinical endocrinology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay. [electronic resource] by Vieira, Teresa C Dias da Silva, Magnus R Cerutti, Janete M Brunner, Elisa Borges, Mariana Arnaldi, Liliane T Kopp, Peter Abucham, Julio Producer: 20030211 In: The Journal of clinical endocrinology and metabolism vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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