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Page 1
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.
Cassatella D, Howard SR, Acierno JS, Xu C, Papadakis GE, Santoni FA, Dwyer AA, Santini S, Sykiotis GP, Chambion C, Meylan J, Marino L, Favre L, Li J, Liu X, Zhang J, Bouloux PM, Geyter C, Paepe A, Dhillo WS, Ferrara JM, Hauschild M, Lang-Muritano M, Lemke JR, Flück C, Nemeth A, Phan-Hug F, Pignatelli D, Popovic V, Pekic S, Quinton R, Szinnai G, l'Allemand D, Konrad D, Sharif S, Iyidir ÖT, Stevenson BJ, Yang H, Dunkel L, Pitteloud N. Cassatella D, et al. Among authors: quinton r. Eur J Endocrinol. 2018 Apr;178(4):377-388. doi: 10.1530/EJE-17-0568. Epub 2018 Feb 1. Eur J Endocrinol. 2018. PMID: 29419413 Free PMC article.
Unilateral renal aplasia in X-linked Kallmann's syndrome.
Kirk JM, Grant DB, Besser GM, Shalet S, Quinton R, Smith CS, White M, Edwards O, Bouloux PM. Kirk JM, et al. Among authors: quinton r. Clin Genet. 1994 Sep;46(3):260-2. doi: 10.1111/j.1399-0004.1994.tb04238.x. Clin Genet. 1994. PMID: 7820942
Kallmann's syndrome.
Bouloux PM, Duke VM, Hall-Craggs M, Manning P, Quinton R, Jacobs HS. Bouloux PM, et al. Among authors: quinton r. Curr Opin Obstet Gynecol. 1994 Jun;6(3):301-3. doi: 10.1097/00001703-199406000-00016. Curr Opin Obstet Gynecol. 1994. PMID: 8038419 No abstract available.
275 results