Tohma T - Search Results

1

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: tohma t. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.

2

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Ohta T, Tohma T, Soejima H, Fukushima Y, Nagai T, Yoshiura K, Jinno Y, Niikawa N. Ohta T, et al. Among authors: tohma t. Hum Genet. 1993 Aug;92(1):1-5. doi: 10.1007/BF00216136. Hum Genet. 1993. PMID: 8365720

3

Inverted insertion of chromosome 7q and ectrodactyly.

Naritomi K, Izumikawa Y, Tohma T, Hirayama K. Naritomi K, et al. Among authors: tohma t. Am J Med Genet. 1993 Jun 15;46(5):492-3. doi: 10.1002/ajmg.1320460505. Am J Med Genet. 1993. PMID: 8322806

4

Characterization of marker chromosomes by fish using microdissected probes from old Carnoy-fixed cells: report of two cases.

Chinen Y, Tohma T, Izumikawa Y, Naritomi K, Hirayama K. Chinen Y, et al. Among authors: tohma t. Jpn J Hum Genet. 1997 Dec;42(4):543-9. doi: 10.1007/BF02767032. Jpn J Hum Genet. 1997. PMID: 9560955

5

Cosmid clones from microdissected human chromosomal region 15q11-q13.

Tohma T, Tamura T, Ohta T, Soejima H, Kubota T, Jinno Y, Tsukamoto K, Nakamura Y, Naritomi K, Niikawa N. Tohma T, et al. Jpn J Hum Genet. 1993 Sep;38(3):267-75. doi: 10.1007/BF01874137. Jpn J Hum Genet. 1993. PMID: 8260719

6

Small interstitial deletion of the long arm of chromosome 2 (2q24.3): further delineation of 2q medial monosomy syndrome.

Chinen Y, Tohma T, Izumikawa Y, Iha T, Goya Y, Naritomi K. Chinen Y, et al. Among authors: tohma t. Jpn J Hum Genet. 1996 Sep;41(3):323-8. doi: 10.1007/BF01913175. Jpn J Hum Genet. 1996. PMID: 8996968

7

Megalocornea-mental retardation syndrome: an additional case report.

Naritomi K, Chinen Y, Tohma T. Naritomi K, et al. Among authors: tohma t. Jpn J Hum Genet. 1997 Sep;42(3):461-5. doi: 10.1007/BF02766950. Jpn J Hum Genet. 1997. PMID: 12503196

8

Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation.

Akiyama M, Kawame H, Ohashi H, Tohma T, Ohta H, Shishikura A, Miyata I, Usui N, Eto Y. Akiyama M, et al. Among authors: tohma t. Am J Med Genet. 2001 Mar 1;99(2):111-4. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1150>3.0.co;2-c. Am J Med Genet. 2001. PMID: 11241467 Review.

9

The Costello syndrome: a boy with thick mitral valves and arrhythmias.

Izumikawa Y, Naritomi K, Tohma T, Shiroma N, Hirayama K. Izumikawa Y, et al. Among authors: tohma t. Jpn J Hum Genet. 1993 Sep;38(3):329-34. doi: 10.1007/BF01874143. Jpn J Hum Genet. 1993. PMID: 7505126 Review.

10

Delineation of the da-Silva syndrome.

Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K. Naritomi K, et al. Among authors: tohma t. Am J Med Genet. 1994 Feb 1;49(3):313-6. doi: 10.1002/ajmg.1320490314. Am J Med Genet. 1994. PMID: 8209892 Review.

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