Ikeuchi T - Search Results

1

Dermatoglyphic development on the volar pads of rats with chromosome abnormalities.

Okajima M, Yosida TH, Ikeuchi T. Okajima M, et al. Among authors: ikeuchi t. Am J Med Genet. 1987 Dec;28(4):1007-13. doi: 10.1002/ajmg.1320280428. Am J Med Genet. 1987. PMID: 3688013

2

Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2.

Arai E, Ikeuchi T, Karasawa S, Tamura A, Yamamoto K, Kida M, Ichimura K, Yuasa Y, Tonomura A. Arai E, et al. Among authors: ikeuchi t. Am J Med Genet. 1992 Sep 15;44(2):163-7. doi: 10.1002/ajmg.1320440209. Am J Med Genet. 1992. PMID: 1456285

3

Chromosome rearrangements at 12q13 in two cases of chondrosarcomas.

Hirabayashi Y, Yoshida MA, Ikeuchi T, Ishida T, Kojima T, Higaki S, Machinami R, Tonomura A. Hirabayashi Y, et al. Among authors: ikeuchi t. Cancer Genet Cytogenet. 1992 May;60(1):35-40. doi: 10.1016/0165-4608(92)90230-6. Cancer Genet Cytogenet. 1992. PMID: 1591704

4

B-cell lineage acute lymphoblastic leukemia with i(7q) and t(9;9)(p22;p24).

Takeda T, Takagi A, Zaike Y, Hirai M, Kawakami M, Mori M, Ohyashiki K, Ikeuchi T. Takeda T, et al. Among authors: ikeuchi t. Cancer Genet Cytogenet. 1988 Feb;30(2):295-9. doi: 10.1016/0165-4608(88)90198-7. Cancer Genet Cytogenet. 1988. PMID: 2963687

5

Rearrangements of chromosome 3 in nonfamilial renal cell carcinomas from Japanese patients.

Yoshida MA, Ikeuchi T, Tachibana Y, Takagi K, Moriyama M, Tonomura A. Yoshida MA, et al. Among authors: ikeuchi t. Jpn J Cancer Res. 1988 May;79(5):600-7. doi: 10.1111/j.1349-7006.1988.tb00029.x. Jpn J Cancer Res. 1988. PMID: 3136112 Free PMC article.

6

Cytogenetic analysis of 23 Japanese patients with amyotrophic lateral sclerosis.

Kaneko K, Saito F, Sunohara N, Ikeuchi T. Kaneko K, et al. Among authors: ikeuchi t. Clin Genet. 1995 Mar;47(3):158-60. doi: 10.1111/j.1399-0004.1995.tb03950.x. Clin Genet. 1995. PMID: 7634540

7

Mapping of the newly identified biliverdin-IX beta reductase gene (BLVRB) to human chromosome 19q13.13-->q13.2 by fluorescence in situ hybridization.

Saito F, Yamaguchi T, Komuro A, Tobe T, Ikeuchi T, Tomita M, Nakajima H. Saito F, et al. Among authors: ikeuchi t. Cytogenet Cell Genet. 1995;71(2):179-81. doi: 10.1159/000134102. Cytogenet Cell Genet. 1995. PMID: 7656592

8

Translocation (9;22)(q22;q12). A recurrent chromosome abnormality in extraskeletal myxoid chondrosarcoma.

Hirabayashi Y, Ishida T, Yoshida MA, Kojima T, Ebihara Y, Machinami R, Ikeuchi T. Hirabayashi Y, et al. Among authors: ikeuchi t. Cancer Genet Cytogenet. 1995 May;81(1):33-7. doi: 10.1016/0165-4608(94)00201-0. Cancer Genet Cytogenet. 1995. PMID: 7773957

9

Chromosome 1q terminal deletion resulting from de novo translocation with an acrocentric chromosome.

Arai E, Nishimura S, Tamura K, Kida M, Ikeuchi T. Arai E, et al. Among authors: ikeuchi t. Jpn J Hum Genet. 1994 Dec;39(4):433-7. doi: 10.1007/BF01892389. Jpn J Hum Genet. 1994. PMID: 7873756

10

Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2).

Arai E, Ikeuchi T, Nakamura Y. Arai E, et al. Among authors: ikeuchi t. Hum Mol Genet. 1994 Jun;3(6):937-9. doi: 10.1093/hmg/3.6.937. Hum Mol Genet. 1994. PMID: 7951241

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