Koyama K - Search Results

1

A high-resolution cytogenetic map of human chromosome 12: localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization.

Takahashi E, Koyama K, Hitomi A, Nakamura Y. Takahashi E, et al. Among authors: koyama k. Hum Genet. 1993 Oct;92(4):405-9. doi: 10.1007/BF01247345. Hum Genet. 1993. PMID: 8225322

2

A high-resolution cytogenetic map of human chromosome 9: localization of 203 new cosmid markers by direct R-banding fluorescence in situ hybridization.

Takahashi E, Koyama K, Hitomi A, Itoh H, Nakamura Y. Takahashi E, et al. Among authors: koyama k. Genomics. 1994 Jan 15;19(2):373-5. doi: 10.1006/geno.1994.1073. Genomics. 1994. PMID: 8188268

3

Isolation and mapping of 328 new cosmid markers on human chromosome 8: construction of a high-resolution cytogenetic map of chromosome 8 with 416 markers.

Nakamura Y, Okui K, Takahashi E, Koyama K. Nakamura Y, et al. Among authors: koyama k. Cytogenet Cell Genet. 1994;65(1-2):115-8. doi: 10.1159/000133614. Cytogenet Cell Genet. 1994. PMID: 8404062

4

Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3.

Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y. Nakagawa H, et al. Among authors: koyama k. Hum Genet. 1998 Feb;102(2):203-6. doi: 10.1007/s004390050678. Hum Genet. 1998. PMID: 9521590

5

A high-resolution cytogenetic map of human chromosome 2: localization of 434 cosmid markers by direct R-banding fluorescence in situ hybridization.

Takahashi E, Koyama K, Hirai M, Itoh H, Nakamura Y. Takahashi E, et al. Among authors: koyama k. Cytogenet Cell Genet. 1995;68(1-2):112-4. doi: 10.1159/000133902. Cytogenet Cell Genet. 1995. PMID: 7956348

6

Isolation and mapping of 88 new RFLP markers on human chromosome 8.

Emi M, Takahashi E, Koyama K, Okui K, Oshimura M, Nakamura Y. Emi M, et al. Among authors: koyama k. Genomics. 1992 Aug;13(4):1261-6. doi: 10.1016/0888-7543(92)90044-s. Genomics. 1992. PMID: 1354643

7

The human homologue of the murine Llglh gene (LLGL) maps within the Smith-Magenis syndrome region in 17p11.2.

Koyama K, Fukushima Y, Inazawa J, Tomotsune D, Takahashi N, Nakamura Y. Koyama K, et al. Cytogenet Cell Genet. 1996;72(1):78-82. doi: 10.1159/000134167. Cytogenet Cell Genet. 1996. PMID: 8565641

8

Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI.

Aihara T, Miyoshi Y, Koyama K, Suzuki M, Takahashi E, Monden M, Nakamura Y. Aihara T, et al. Among authors: koyama k. Cytogenet Cell Genet. 1998;81(3-4):191-3. doi: 10.1159/000015027. Cytogenet Cell Genet. 1998. PMID: 9730600

9

VNTR (variable number of tandem repeat) sequences as transcriptional, translational, or functional regulators.

Nakamura Y, Koyama K, Matsushima M. Nakamura Y, et al. Among authors: koyama k. J Hum Genet. 1998;43(3):149-52. doi: 10.1007/s100380050059. J Hum Genet. 1998. PMID: 9747025 Review.

10

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome.

Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Matsuura N, Monden M, Nakamura Y. Nakagawa H, et al. Among authors: koyama k. Hum Genet. 1998 Aug;103(2):168-72. doi: 10.1007/s004390050801. Hum Genet. 1998. PMID: 9760200

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,748 results

Search Page

Filters