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Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.
Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Yoshida R, et al. Among authors: hasegawa t, hasegawa y. J Clin Endocrinol Metab. 2004 Jul;89(7):3359-64. doi: 10.1210/jc.2003-032091. J Clin Endocrinol Metab. 2004. PMID: 15240615
Two novel and one recurrent PTPN11 mutations in LEOPARD syndrome.
Yoshida R, Nagai T, Hasegawa T, Kinoshita E, Tanaka T, Ogata T. Yoshida R, et al. Among authors: hasegawa t. Am J Med Genet A. 2004 Nov 1;130A(4):432-4. doi: 10.1002/ajmg.a.30281. Am J Med Genet A. 2004. PMID: 15389709 No abstract available.
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.
Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. Fukami M, et al. Among authors: hasegawa t. J Clin Endocrinol Metab. 2005 Jan;90(1):414-26. doi: 10.1210/jc.2004-0810. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483095
6,443 results