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Molecular pathology of Shprintzen-Goldberg syndrome.
Kosaki K, Takahashi D, Udaka T, Kosaki R, Matsumoto M, Ibe S, Isobe T, Tanaka Y, Takahashi T. Kosaki K, et al. Among authors: udaka t. Am J Med Genet A. 2006 Jan 1;140(1):104-8; author reply 109-10. doi: 10.1002/ajmg.a.31006. Am J Med Genet A. 2006. PMID: 16333834 No abstract available.
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: udaka t. J Pediatr. 2006 Mar;148(3):410-4. doi: 10.1016/j.jpeds.2005.10.044. J Pediatr. 2006. PMID: 16615981
DHPLC in clinical molecular diagnostic services.
Kosaki K, Udaka T, Okuyama T. Kosaki K, et al. Among authors: udaka t. Mol Genet Metab. 2005 Sep-Oct;86(1-2):117-23. doi: 10.1016/j.ymgme.2005.07.033. Mol Genet Metab. 2005. PMID: 16202954 Review.
75 results