Yamamori S - Search Results

1

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.

2

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

3

Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature.

Uehara S, Hanew K, Harada N, Yamamori S, Nata M, Niikawa N, Okamura K. Uehara S, et al. Among authors: yamamori s. Am J Med Genet. 2001 Mar 15;99(3):196-9. doi: 10.1002/1096-8628(20010315)99:3<196::aid-ajmg1157>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11241489

4

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

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

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

7

A late-appearing Philadelphia chromosome in acute lymphoblastic leukemia confirmed by expression of BCR-ABL mRNA.

Tsuchiya H, Migita M, Yamamori S, Kaneko Y, Adachi N, Nakamura T, Nobukuni Y, el-Sonbaty SS, Matsuda I. Tsuchiya H, et al. Among authors: yamamori s. Leukemia. 1995 Oct;9(10):1689-93. Leukemia. 1995. PMID: 7564511

8

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

9

Impaired G-CSF production at post-transcriptional level in a patient with chronic idiopathic neutropenia.

Morikawa K, Yamamori S, Oiwa K, Morikawa S, Oseko F, Kubota T, Nakamura T. Morikawa K, et al. Among authors: yamamori s. Br J Haematol. 1993 Sep;85(1):200-2. doi: 10.1111/j.1365-2141.1993.tb08671.x. Br J Haematol. 1993. PMID: 7504508

10

Clinical significance of TAL1 gene alteration in childhood T-cell acute lymphoblastic leukemia and lymphoma.

Kikuchi A, Hayashi Y, Kobayashi S, Hanada R, Moriwaki K, Yamamoto K, Fujimoto J, Kaneko Y, Yamamori S. Kikuchi A, et al. Among authors: yamamori s. Leukemia. 1993 Jul;7(7):933-8. Leukemia. 1993. PMID: 8321044

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