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Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.
Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Takahashi T, Fukushima Y, Kawame H, Kosaki K. Aramaki M, et al. Among authors: takahashi t. J Pediatr. 2006 Mar;148(3):410-4. doi: 10.1016/j.jpeds.2005.10.044. J Pediatr. 2006. PMID: 16615981
Complete mutation analysis panel of the 39 human HOX genes.
Kosaki K, Kosaki R, Suzuki T, Yoshihashi H, Takahashi T, Sasaki K, Tomita M, McGinnis W, Matsuo N. Kosaki K, et al. Among authors: takahashi t. Teratology. 2002 Feb;65(2):50-62. doi: 10.1002/tera.10009. Teratology. 2002. PMID: 11857506
Hyperinsulinemic hypoglycemia in a newborn infant with trisomy 13.
Tamame T, Hori N, Homma H, Yoshida R, Inokuchi M, Kosaki K, Takahashi T, Hasegawa T. Tamame T, et al. Among authors: takahashi t. Am J Med Genet A. 2004 Sep 1;129A(3):321-2. doi: 10.1002/ajmg.a.30147. Am J Med Genet A. 2004. PMID: 15326637 No abstract available.
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