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	1.	The challenge of mistaken sex assignment in an 11-year-old with virilizing CAH. [electronic resource] by Taboada, Martha Gagliardi, Priscila Producer: 20110930 In: Advances in experimental medicine and biology vol. 707 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Quality of Life in Adolescent Boys with Idiopathic Short Stature: Positive Impact of Growth Hormone and Aromatase Inhibitors. [electronic resource] by Bullinger, Monika Bloemeke, Janika Mericq, Veronica Sommer, Rachel Gaete, Xiemena Ross, Judith L Yu, Y Miles Permuy, Joseph Gagliardi, Priscila Damaso, Y Ligeia Mauras, Nelly Producer: 20190801 In: Hormone research in paediatrics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Randomized Trial of Aromatase Inhibitors, Growth Hormone, or Combination in Pubertal Boys with Idiopathic, Short Stature. [electronic resource] by Mauras, Nelly Ross, Judith L Gagliardi, Priscila Yu, Y Miles Hossain, Jobayer Permuy, Joseph Damaso, Ligeia Merinbaum, Debbie Singh, Ravinder J Gaete, Ximena Mericq, Veronica Producer: 20170719 In: The Journal of clinical endocrinology and metabolism vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Central precocious puberty caused by mutations in the imprinted gene MKRN3. [electronic resource] by Abreu, Ana Paula Dauber, Andrew Macedo, Delanie B Noel, Sekoni D Brito, Vinicius N Gill, John C Cukier, Priscilla Thompson, Iain R Navarro, Victor M Gagliardi, Priscila C Rodrigues, Tânia Kochi, Cristiane Longui, Carlos Alberto Beckers, Dominique de Zegher, Francis Montenegro, Luciana R Mendonca, Berenice B Carroll, Rona S Hirschhorn, Joel N Latronico, Ana Claudia Kaiser, Ursula B Producer: 20130716 In: The New England journal of medicine vol. 368 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	CLCN2 chloride channel mutations in familial hyperaldosteronism type II. [electronic resource] by Scholl, Ute I Stölting, Gabriel Schewe, Julia Thiel, Anne Tan, Hua Nelson-Williams, Carol Vichot, Alfred A Jin, Sheng Chih Loring, Erin Untiet, Verena Yoo, Taekyeong Choi, Jungmin Xu, Shengxin Wu, Aihua Kirchner, Marieluise Mertins, Philipp Rump, Lars C Onder, Ali Mirza Gamble, Cory McKenney, Daniel Lash, Robert W Jones, Deborah P Chune, Gary Gagliardi, Priscila Choi, Murim Gordon, Richard Stowasser, Michael Fahlke, Christoph Lifton, Richard P Producer: 20190510 In: Nature genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)