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	1.	Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations. [electronic resource] by Pardo, Viviane Rubio, Ileana G S Knobel, Meyer Aguiar-Oliveira, Manoel H Santos, Marcos M Gomes, Simone A Oliveira, Carla R P Targovnik, Hector M Medeiros-Neto, Geraldo Producer: 20081003 In: Thyroid : official journal of the American Thyroid Association vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Growth or somatotrophic hormone: new perspectives in isolated GH deficiency after description of the mutation in the GHRH receptor gene in individuals of Itabaianinha County, Brazil]. [electronic resource] by Souza, Anita Hermínia O Salvatori, Roberto Martinelli, Carlos E Carvalho, Walter M O Menezes, Carlos A Barretto, Elenilde S de A Barreto Filho, José A S Alcântara, Marta R S de Oliveira, Carla R P Alcântara, Paula R S de Ramalho, Roberto J R Oliveira, Hélio A Lima, Ivana B de Carneiro, Jamille N Santos, Marcos M Gill, Matthew S Clayton, Peter E Oliveira, Manuel H A Producer: 20050503 In: Arquivos brasileiros de endocrinologia e metabologia vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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