Okuyama T - Search Results

1

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: okuyama t. J Hum Genet. 2007;52(5):397-405. doi: 10.1007/s10038-007-0127-4. Epub 2007 Apr 4. J Hum Genet. 2007. PMID: 17406783

2

[Genetic medicine in Japan].

Okuyama T, Kosaki R, Fukuhara Y. Okuyama T, et al. Nihon Rinsho. 2005 Mar;63(3):403-7. Nihon Rinsho. 2005. PMID: 15773337 Review. Japanese.

3

OEIS complex with del(3)(q12.2q13.2).

Kosaki R, Fukuhara Y, Kosuga M, Okuyama T, Kawashima N, Honna T, Ueoka K, Kosaki K. Kosaki R, et al. Among authors: okuyama t. Am J Med Genet A. 2005 Jun 1;135(2):224-6. doi: 10.1002/ajmg.a.30733. Am J Med Genet A. 2005. PMID: 15887303 Review. No abstract available.

4

Histopathological and behavioral improvement of murine mucopolysaccharidosis type VII by intracerebral transplantation of neural stem cells.

Fukuhara Y, Li XK, Kitazawa Y, Inagaki M, Matsuoka K, Kosuga M, Kosaki R, Shimazaki T, Endo H, Umezawa A, Okano H, Takahashi T, Okuyama T. Fukuhara Y, et al. Among authors: okuyama t. Mol Ther. 2006 Mar;13(3):548-55. doi: 10.1016/j.ymthe.2005.09.020. Epub 2005 Nov 28. Mol Ther. 2006. PMID: 16316785 Free article.

5

Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.

Kosaki R, Hanai S, Kakishima H, Okada MA, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T. Kosaki R, et al. Among authors: okuyama t. Congenit Anom (Kyoto). 2006 Jun;46(2):115-7. doi: 10.1111/j.1741-4520.2006.00111.x. Congenit Anom (Kyoto). 2006. PMID: 16732770

6

Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of the FMR2 gene.

Honda S, Hayashi S, Kato M, Niida Y, Hayasaka K, Okuyama T, Imoto I, Mizutani S, Inazawa J. Honda S, et al. Among authors: okuyama t. Am J Med Genet A. 2007 Apr 1;143A(7):687-93. doi: 10.1002/ajmg.a.31638. Am J Med Genet A. 2007. PMID: 17343270

7

Monozygotic twins of Smith-Magenis syndrome.

Kosaki R, Okuyama T, Tanaka T, Migita O, Kosaki K. Kosaki R, et al. Among authors: okuyama t. Am J Med Genet A. 2007 Apr 1;143A(7):768-9. doi: 10.1002/ajmg.a.31647. Am J Med Genet A. 2007. PMID: 17345621 No abstract available.

8

The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.

Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J. Hayashi S, et al. Among authors: okuyama t. Am J Med Genet A. 2008 Aug 15;146A(16):2145-51. doi: 10.1002/ajmg.a.32433. Am J Med Genet A. 2008. PMID: 18629876

9

Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype-phenotype correlation.

Otomo T, Muramatsu T, Yorifuji T, Okuyama T, Nakabayashi H, Fukao T, Ohura T, Yoshino M, Tanaka A, Okamoto N, Inui K, Ozono K, Sakai N. Otomo T, et al. Among authors: okuyama t. J Hum Genet. 2009 Mar;54(3):145-51. doi: 10.1038/jhg.2009.3. Epub 2009 Feb 6. J Hum Genet. 2009. PMID: 19197337

10

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.

Hayashi S, Imoto I, Aizu Y, Okamoto N, Mizuno S, Kurosawa K, Okamoto N, Honda S, Araki S, Mizutani S, Numabe H, Saitoh S, Kosho T, Fukushima Y, Mitsubuchi H, Endo F, Chinen Y, Kosaki R, Okuyama T, Ohki H, Yoshihashi H, Ono M, Takada F, Ono H, Yagi M, Matsumoto H, Makita Y, Hata A, Inazawa J. Hayashi S, et al. Among authors: okuyama t. J Hum Genet. 2011 Feb;56(2):110-24. doi: 10.1038/jhg.2010.129. Epub 2010 Oct 28. J Hum Genet. 2011. PMID: 20981036

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