Kondo I - Search Results

1

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Greenberg F, Guzzetta V, Montes de Oca-Luna R, Magenis RE, Smith AC, Richter SF, Kondo I, Dobyns WB, Patel PI, Lupski JR. Greenberg F, et al. Among authors: kondo i. Am J Hum Genet. 1991 Dec;49(6):1207-18. Am J Hum Genet. 1991. PMID: 1746552 Free PMC article.

2

Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.

Juyal RC, Kuwano A, Kondo I, Zara F, Baldini A, Patel PI. Juyal RC, et al. Among authors: kondo i. Am J Med Genet. 1996 Dec 11;66(2):193-6. doi: 10.1002/(SICI)1096-8628(19961211)66:2<193::AID-AJMG13>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8958329

3

Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).

Kondo I, Matsuura S, Kuwajima K, Tokashiki M, Izumikawa Y, Naritomi K, Niikawa N, Kajii T. Kondo I, et al. Am J Med Genet. 1991 Nov 1;41(2):225-9. doi: 10.1002/ajmg.1320410219. Am J Med Genet. 1991. PMID: 1785639

4

Familial retinoblastoma (mother and son) with 13q14 deletion.

Fukushima Y, Kuroki Y, Ito T, Kondo I, Nishigaki I. Fukushima Y, et al. Among authors: kondo i. Hum Genet. 1987 Oct;77(2):104-7. doi: 10.1007/BF00272373. Hum Genet. 1987. PMID: 3653883

5

Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.

Deng HX, Abe K, Kondo I, Tsukahara M, Inagaki H, Hamada I, Fukushima Y, Niikawa N. Deng HX, et al. Among authors: kondo i. Hum Genet. 1991 Apr;86(6):541-4. doi: 10.1007/BF00201538. Hum Genet. 1991. PMID: 1673956

6

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.

Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: kondo i. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458

7

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

Meguro M, Kashiwagi A, Mitsuya K, Nakao M, Kondo I, Saitoh S, Oshimura M. Meguro M, et al. Among authors: kondo i. Nat Genet. 2001 May;28(1):19-20. doi: 10.1038/ng0501-19. Nat Genet. 2001. PMID: 11326269

8

Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.

Scheffer H, Kema IP, Kondo I, van der Veen AY, Ikeuchi T, Buys CH. Scheffer H, et al. Among authors: kondo i. Hum Genet. 1987 Dec;77(4):335-7. doi: 10.1007/BF00291421. Hum Genet. 1987. PMID: 2891602

9

Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.

Kondo I, Hamabe J, Yamamoto K, Niikawa N. Kondo I, et al. Clin Genet. 1990 Dec;38(6):422-6. doi: 10.1111/j.1399-0004.1990.tb03607.x. Clin Genet. 1990. PMID: 1981180

10

The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2.

Kimura T, Arakawa Y, Inoue S, Fukushima Y, Kondo I, Koyama K, Hosoi T, Orimo A, Muramatsu M, Nakamura Y, Abe T, Inazawa J. Kimura T, et al. Among authors: kondo i. Am J Med Genet. 1997 Mar 31;69(3):320-4. Am J Med Genet. 1997. PMID: 9096764

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