Kondo I - Search Results

1

Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.

Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I. Masuda N, et al. Among authors: kondo i. J Med Genet. 1995 Sep;32(9):701-5. doi: 10.1136/jmg.32.9.701. J Med Genet. 1995. PMID: 8544189 Free PMC article.

2

Identification of a novel CYP2D6 allele associated with poor metabolism of sparteine in a Japanese population.

Kondo I, Yonaha M, Okano K, Gonzalez FJ, Kanazawa I. Kondo I, et al. Pharmacogenetics. 1991 Dec;1(3):161-4. doi: 10.1097/00008571-199112000-00006. Pharmacogenetics. 1991. PMID: 1688247

3

Laser microdissection and single unique primer PCR allow generation of regional chromosome DNA clones from a single human chromosome.

Hadano S, Watanabe M, Yokoi H, Kogi M, Kondo I, Tsuchiya H, Kanazawa I, Wakasa K, Ikeda JE. Hadano S, et al. Among authors: kondo i. Genomics. 1991 Oct;11(2):364-73. doi: 10.1016/0888-7543(91)90144-4. Genomics. 1991. PMID: 1769652

4

Weaver syndrome in two Japanese children.

Kondo I, Mori Y, Kuwajima K. Kondo I, et al. Am J Med Genet. 1991 Nov 1;41(2):221-4. doi: 10.1002/ajmg.1320410218. Am J Med Genet. 1991. PMID: 1785638 Review.

5

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I. Kondo I, et al. J Med Genet. 1990 Feb;27(2):105-8. doi: 10.1136/jmg.27.2.105. J Med Genet. 1990. PMID: 1969487 Free PMC article.

6

Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families.

Kanazawa I, Kondo I, Ikeda JE, Ikeda T, Shizu Y, Yoshida M, Narabayashi H, Kuroda S, Tsunoda H, Mizuta E, et al. Kanazawa I, et al. Among authors: kondo i. Hum Genet. 1990 Aug;85(3):257-60. doi: 10.1007/BF00206741. Hum Genet. 1990. PMID: 1975553

7

[Genetic aspects of Huntington's chorea].

Kondo I, Kanazawa I. Kondo I, et al. Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):1023-5. Tanpakushitsu Kakusan Koso. 1988. PMID: 2908390 Japanese. No abstract available.

8

A BamHI polymorphism in the human cytochrome P450 gene, CYP2D6.

Morimoto Y, Murayama N, Kuwano A, Yoshimura O, Kondo I. Morimoto Y, et al. Among authors: kondo i. Clin Genet. 1995 Feb;47(2):103-4. doi: 10.1111/j.1399-0004.1995.tb03934.x. Clin Genet. 1995. PMID: 7606840 No abstract available.

9

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation.

Komure O, Sano A, Nishino N, Yamauchi N, Ueno S, Kondoh K, Sano N, Takahashi M, Murayama N, Kondo I, et al. Komure O, et al. Among authors: kondo i. Neurology. 1995 Jan;45(1):143-9. doi: 10.1212/wnl.45.1.143. Neurology. 1995. PMID: 7824105 Clinical Trial.

10

Haplotype analysis at the FRAXA locus in the Japanese population.

Richards RI, Kondo I, Holman K, Yamauchi M, Seki N, Kishi K, Staples A, Sutherland GR, Hori T. Richards RI, et al. Among authors: kondo i. Am J Med Genet. 1994 Jul 15;51(4):412-6. doi: 10.1002/ajmg.1320510422. Am J Med Genet. 1994. PMID: 7943009

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