Yamamoto T - Search Results

1

Investigation of the candidate region for trigonocephaly in a patient with monosomy 9p syndrome using array-CGH.

Shimojima K, Yamamoto T. Shimojima K, et al. Among authors: yamamoto t. Am J Med Genet A. 2009 May;149A(5):1076-80. doi: 10.1002/ajmg.a.32783. Am J Med Genet A. 2009. PMID: 19396833 No abstract available.

2

Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1).

Torisu H, Yamamoto T, Fujiwaki T, Kadota M, Oshimura M, Kurosawa K, Akaboshi S, Oka A. Torisu H, et al. Among authors: yamamoto t. Am J Med Genet A. 2004 Nov 15;131(1):94-8. doi: 10.1002/ajmg.a.30413. Am J Med Genet A. 2004. PMID: 15384094

3

Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23.

Kawara H, Yamamoto T, Harada N, Yoshiura K, Niikawa N, Nishimura A, Mizuguchi T, Matsumoto N. Kawara H, et al. Among authors: yamamoto t. Am J Med Genet A. 2006 Feb 15;140(4):373-7. doi: 10.1002/ajmg.a.31094. Am J Med Genet A. 2006. PMID: 16419130

4

Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome.

Yamamoto T, Sameshima K, Sekido K, Aida N, Matsumoto N, Naritomi K, Kurosawa K. Yamamoto T, et al. Am J Med Genet A. 2006 Jun 15;140(12):1302-4. doi: 10.1002/ajmg.a.31297. Am J Med Genet A. 2006. PMID: 16691595

5

Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits.

Páez MT, Yamamoto T, Hayashi K, Yasuda T, Harada N, Matsumoto N, Kurosawa K, Furutani Y, Asakawa S, Shimizu N, Matsuoka R. Páez MT, et al. Among authors: yamamoto t. Am J Med Genet A. 2008 May 1;146A(9):1158-65. doi: 10.1002/ajmg.a.32205. Am J Med Genet A. 2008. PMID: 18393291

6

Tetralogy of Fallot associated with pulmonary atresia and major aortopulmonary collateral arteries in a patient with interstitial deletion of 16q21-q22.1.

Yamamoto T, Dowa Y, Ueda H, Kawataki M, Asou T, Sasaki Y, Harada N, Matsumoto N, Matsuoka R, Kurosawa K. Yamamoto T, et al. Am J Med Genet A. 2008 Jun 15;146A(12):1575-80. doi: 10.1002/ajmg.a.32204. Am J Med Genet A. 2008. PMID: 18470894

7

Comment on "Altered DNA copy number in patients with different seizure disorder type: by array-CGH" by Kim HS et al. Brain & Development 2007;29:639-643.

Yamamoto T, Páez MT, Shimojima K. Yamamoto T, et al. Brain Dev. 2009 Jan;31(1):94. doi: 10.1016/j.braindev.2008.06.008. Epub 2008 Jul 26. Brain Dev. 2009. PMID: 18657918 No abstract available.

8

Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).

Shimojima K, Páez MT, Kurosawa K, Yamamoto T. Shimojima K, et al. Among authors: yamamoto t. Brain Dev. 2009 Sep;31(8):629-33. doi: 10.1016/j.braindev.2008.08.013. Epub 2008 Oct 5. Brain Dev. 2009. PMID: 18835671

9

Application of array-based comparative genome hybridization in children with developmental delay or mental retardation.

Liang JS, Shimojima K, Yamamoto T. Liang JS, et al. Among authors: yamamoto t. Pediatr Neonatol. 2008 Dec;49(6):213-7. doi: 10.1016/S1875-9572(09)60013-9. Pediatr Neonatol. 2008. PMID: 19166117 Free article. Review.

10

Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.

Shimojima K, Inoue T, Hoshino A, Kakiuchi S, Watanabe Y, Sasaki M, Nishimura A, Takeshita-Yanagisawa A, Tajima G, Ozawa H, Kubota M, Tohyama J, Sasaki M, Oka A, Saito K, Osawa M, Yamamoto T. Shimojima K, et al. Among authors: yamamoto t. Brain Dev. 2010 Mar;32(3):171-9. doi: 10.1016/j.braindev.2009.02.011. Epub 2009 Mar 27. Brain Dev. 2010. PMID: 19328639

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