Niikawa N - Search Results

1

The growth hormone receptor gene mutation of a Japanese patient with Laron syndrome.

Otsuka T, Iwatani N, Kodama M, Sakakida M, Shichiri M, Jinno Y, Niikawa N, Miike T. Otsuka T, et al. Among authors: niikawa n. Jpn J Hum Genet. 1997 Jun;42(2):323-9. doi: 10.1007/BF02766954. Jpn J Hum Genet. 1997. PMID: 9290257

2

Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.

Nagano K, Nakura J, Kihara K, Ye L, Kamino K, Mitsuda N, Ohta T, Jinno Y, Niikawa N, Miki T, et al. Nagano K, et al. Among authors: niikawa n. Jpn J Hum Genet. 1993 Dec;38(4):391-7. doi: 10.1007/BF01907985. Jpn J Hum Genet. 1993. PMID: 8186416

3

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. Among authors: niikawa n. Jpn J Hum Genet. 1993 Sep;38(3):267-75. doi: 10.1007/BF01874137. Jpn J Hum Genet. 1993. PMID: 8260719

4

Dystrophin isoforms expressed in the mouse retina.

Tamura T, Yoshioka K, Jinno Y, Niikawa N, Miike T. Tamura T, et al. Among authors: niikawa n. J Neurol Sci. 1993 Apr;115(2):214-8. doi: 10.1016/0022-510x(93)90227-p. J Neurol Sci. 1993. PMID: 8482981

5

Two polymorphic AvaI and HhaI sites in a differentially methylated region of the human H19 gene.

Miyatake S, Ikeda Y, Jinno Y, Niikawa N. Miyatake S, et al. Among authors: niikawa n. Jpn J Hum Genet. 1996 Jun;41(2):253-5. doi: 10.1007/BF01875986. Jpn J Hum Genet. 1996. PMID: 8771991

6

Isolation of 2 novel RFLP markers and their localization at 2q35 by microdissection and subsequent enzymatic amplification.

Kibe T, Tsukamoto K, Hirota T, Yoshiura K, Ohta T, Tohma T, Tamura T, Jinno Y, Niikawa N. Kibe T, et al. Among authors: niikawa n. Jpn J Hum Genet. 1992 Dec;37(4):263-70. doi: 10.1007/BF01883317. Jpn J Hum Genet. 1992. PMID: 1284292

7

Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Deng HX, Yoshiura K, Dirks RW, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N. Deng HX, et al. Among authors: niikawa n. Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034. Hum Genet. 1992. PMID: 1577461

8

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.

Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N. Sugino S, et al. Among authors: niikawa n. Am J Med Genet. 1989 Dec;34(4):555-61. doi: 10.1002/ajmg.1320340421. Am J Med Genet. 1989. PMID: 2576185

9

Six dinucleotide repeat polymorphisms on chromosome 7.

Nakura J, Miki T, Ye L, Mitsuda N, Ogihara T, Ohta T, Jinno Y, Niikawa N, Takahashi-Fujii A, Ishino Y. Nakura J, et al. Among authors: niikawa n. Jpn J Hum Genet. 1994 Dec;39(4):447-9. doi: 10.1007/BF01892393. Jpn J Hum Genet. 1994. PMID: 7873760 No abstract available.

10

Population variation in the dinucleotide repeat polymorphism at the D8S360 locus.

Kamino K, Nakura J, Kihara K, Ye L, Nagano K, Ohta T, Jinno Y, Niikawa N, Miki T, Ogihara T. Kamino K, et al. Among authors: niikawa n. Hum Mol Genet. 1993 Oct;2(10):1751. doi: 10.1093/hmg/2.10.1751. Hum Mol Genet. 1993. PMID: 8268949 No abstract available.

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