Yamamori S - Search Results

1

Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome.

Kondo Y, Mizuno S, Ohara K, Nakamura T, Yamada K, Yamamori S, Hayakawa C, Ishii T, Yamada Y, Wakamatsu N. Kondo Y, et al. Among authors: yamamori s. Am J Med Genet A. 2006 Feb 1;140(3):227-32. doi: 10.1002/ajmg.a.31073. Am J Med Genet A. 2006. PMID: 16411203

2

Detection of aberrations of ubiquitin-conjugating enzyme E2C gene (UBE2C) in advanced colon cancer with liver metastases by DNA microarray and two-color FISH.

Takahashi Y, Ishii Y, Nishida Y, Ikarashi M, Nagata T, Nakamura T, Yamamori S, Asai S. Takahashi Y, et al. Among authors: yamamori s. Cancer Genet Cytogenet. 2006 Jul 1;168(1):30-5. doi: 10.1016/j.cancergencyto.2005.12.011. Cancer Genet Cytogenet. 2006. PMID: 16772118

3

Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1).

Hiraki Y, Fujita H, Yamamori S, Ohashi H, Eguchi M, Harada N, Mizuguchi T, Matsumoto N. Hiraki Y, et al. Among authors: yamamori s. Am J Med Genet A. 2006 Aug 15;140(16):1773-7. doi: 10.1002/ajmg.a.31364. Am J Med Genet A. 2006. PMID: 16835918

4

9q34.3 deletion syndrome in three unrelated children.

Iwakoshi M, Okamoto N, Harada N, Nakamura T, Yamamori S, Fujita H, Niikawa N, Matsumoto N. Iwakoshi M, et al. Among authors: yamamori s. Am J Med Genet A. 2004 Apr 30;126A(3):278-83. doi: 10.1002/ajmg.a.20602. Am J Med Genet A. 2004. PMID: 15054842 Review.

5

Microdeletion in the SHOX 3' region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: implication for the SHOX enhancer.

Fukami M, Okuyama T, Yamamori S, Nishimura G, Ogata T. Fukami M, et al. Among authors: yamamori s. Am J Med Genet A. 2005 Aug 15;137(1):72-6. doi: 10.1002/ajmg.a.30852. Am J Med Genet A. 2005. PMID: 16007631 Review.

6

Molecular genetic alterations and gene expression profile of a malignant rhabdoid tumor of the kidney.

Nagata T, Takahashi Y, Ishii Y, Asai S, Sugahara-Kobayashi M, Nishida Y, Murata A, Yamamori S, Ogawa Y, Nakamura T, Murakami H, Nakamura M, Shichino H, Chin M, Sugito K, Ikeda T, Koshinaga T, Mugishima H. Nagata T, et al. Among authors: yamamori s. Cancer Genet Cytogenet. 2005 Dec;163(2):130-7. doi: 10.1016/j.cancergencyto.2005.05.009. Cancer Genet Cytogenet. 2005. PMID: 16337855

7

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients.

Muto R, Yamamori S, Ohashi H, Osawa M. Muto R, et al. Among authors: yamamori s. Am J Med Genet. 2002 Apr 1;108(4):285-9. doi: 10.1002/ajmg.10094. Am J Med Genet. 2002. PMID: 11920832

8

Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism.

Shimizu R, Mitsui N, Mori Y, Cho S, Yamamori S, Osawa M, Ohashi H. Shimizu R, et al. Among authors: yamamori s. Am J Med Genet A. 2008 Jun 1;146A(11):1458-61. doi: 10.1002/ajmg.a.32319. Am J Med Genet A. 2008. PMID: 18449926

9

Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy.

Shiihara T, Kato M, Kimura T, Hayasaka K, Yamamori S, Ogata T. Shiihara T, et al. Among authors: yamamori s. Am J Med Genet A. 2004 Jul 15;128A(2):214-6. doi: 10.1002/ajmg.a.20552. Am J Med Genet A. 2004. PMID: 15214020 No abstract available.

10

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC, Ishino F, Ogata T. Kagami M, et al. Among authors: yamamori s. Nat Genet. 2008 Feb;40(2):237-42. doi: 10.1038/ng.2007.56. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176563

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