Tsuji K - Search Results

1

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.

Narahara K, Tsuji K, Yokoyama Y, Namba H, Murakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, et al. Narahara K, et al. Among authors: tsuji k. Am J Med Genet. 1991 Sep 1;40(3):348-53. doi: 10.1002/ajmg.1320400322. Am J Med Genet. 1991. PMID: 1951444

2

Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.

Kobayashi T, Narahara K, Yokoyama Y, Ueyama S, Mohri O, Fujii T, Fujimoto M, Ohtsuki S, Tsuji K, Seino Y. Kobayashi T, et al. Among authors: tsuji k. Am J Med Genet. 1991 Dec 15;41(4):460-3. doi: 10.1002/ajmg.1320410416. Am J Med Genet. 1991. PMID: 1776638 Review.

3

Assignment of human porphobilinogen deaminase to 11q24.1----q24.2 by in situ hybridization and gene dosage studies.

Namba H, Narahara K, Tsuji K, Yokoyama Y, Seino Y. Namba H, et al. Among authors: tsuji k. Cytogenet Cell Genet. 1991;57(2-3):105-8. doi: 10.1159/000133123. Cytogenet Cell Genet. 1991. PMID: 1914516

4

Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.

Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H. Narahara K, et al. Among authors: tsuji k. Am J Med Genet. 1990 Feb;35(2):269-73. doi: 10.1002/ajmg.1320350225. Am J Med Genet. 1990. PMID: 2178418 Review.

5

Acampomelic campomelic syndrome and sex reversal associated with de novo t(12;17) translocation.

Ninomiya S, Narahara K, Tsuji K, Yokoyama Y, Ito S, Seino Y. Ninomiya S, et al. Among authors: tsuji k. Am J Med Genet. 1995 Mar 13;56(1):31-4. doi: 10.1002/ajmg.1320560109. Am J Med Genet. 1995. PMID: 7747782 Review.

6

Craniosynostosis and hemizygosity for D7S135 caused by a de novo and apparently balanced t(6;7) translocation.

Tsuji K, Narahara K, Kikkawa K, Murakami M, Yokoyama Y, Ninomiya S, Seino Y. Tsuji K, et al. Am J Med Genet. 1994 Jan 1;49(1):98-102. doi: 10.1002/ajmg.1320490119. Am J Med Genet. 1994. PMID: 7909651

7

Reproductive risk in mating between two translocation carriers: case report and review of the literature.

Tsuji K, Narahara K, Yokoyama Y, Ninomiya S, Yonesawa S, Hiramatsu Y, Masaoka H, Kudo N, Seino Y. Tsuji K, et al. Am J Med Genet. 1993 Jun 15;46(5):524-8. doi: 10.1002/ajmg.1320460513. Am J Med Genet. 1993. PMID: 8322814 Review.

8

45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individuals.

Teraoka M, Narahara K, Yokoyama Y, Tsuji K, Kikkawa K, Ito S, Koyama K, Seino Y. Teraoka M, et al. Among authors: tsuji k. Am J Med Genet. 1998 Aug 6;78(5):424-8. doi: 10.1002/(sici)1096-8628(19980806)78:5<424::aid-ajmg6>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9714008

9

Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.

Narahara K, Takahashi Y, Murakami M, Tsuji K, Yokoyama Y, Murakami R, Ninomiya S, Seino Y. Narahara K, et al. Among authors: tsuji k. J Med Genet. 1992 Jun;29(6):432-3. doi: 10.1136/jmg.29.6.432. J Med Genet. 1992. PMID: 1352356 Free PMC article. Review.

10

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation.

Yokoyama Y, Narahara K, Tsuji K, Ninomiya S, Seino Y. Yokoyama Y, et al. Among authors: tsuji k. Hum Genet. 1992 Sep-Oct;90(1-2):177-8. doi: 10.1007/BF00210770. Hum Genet. 1992. PMID: 1427774

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