Ohta T - Search Results

1

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Ohta T, Tohma T, Soejima H, Fukushima Y, Nagai T, Yoshiura K, Jinno Y, Niikawa N. Ohta T, et al. Hum Genet. 1993 Aug;92(1):1-5. doi: 10.1007/BF00216136. Hum Genet. 1993. PMID: 8365720

2

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: ohta t. Jpn J Hum Genet. 1993 Sep;38(3):267-75. doi: 10.1007/BF01874137. Jpn J Hum Genet. 1993. PMID: 8260719

3

Functional complementation in mouse-human radiation hybrids assigns the putative murine scid gene to the pericentric region of human chromosome 8.

Komatsu K, Ohta T, Jinno Y, Niikawa N, Okumura Y. Komatsu K, et al. Among authors: ohta t. Hum Mol Genet. 1993 Jul;2(7):1031-4. doi: 10.1093/hmg/2.7.1031. Hum Mol Genet. 1993. PMID: 8364539

4

Mapping of the bone morphogenetic protein 1 gene (BMP1) to 8p21: removal of BMP1 from candidacy for the bone disorder in Langer-Giedion syndrome.

Yoshiura K, Tamura T, Hong HS, Ohta T, Soejima H, Kishino T, Jinno Y, Niikawa N. Yoshiura K, et al. Among authors: ohta t. Cytogenet Cell Genet. 1993;64(3-4):208-9. doi: 10.1159/000133577. Cytogenet Cell Genet. 1993. PMID: 8404039

5

Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis.

Ohta T, Nakano M, Tsujita T, Abe K, Osoegawa K, Yamagata T, Yoshiura K, Jinno Y, Soeda E, Nakamura Y, Niikawa N. Ohta T, et al. Am J Hum Genet. 1996 Mar;58(3):544-50. Am J Hum Genet. 1996. PMID: 8644714 Free PMC article.

6

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: ohta t. Jpn J Hum Genet. 1993 Dec;38(4):391-7. doi: 10.1007/BF01907985. Jpn J Hum Genet. 1993. PMID: 8186416

7

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: ohta t. Jpn J Hum Genet. 1992 Dec;37(4):263-70. doi: 10.1007/BF01883317. Jpn J Hum Genet. 1992. PMID: 1284292

8

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I.

Tsukamoto K, Tohma T, Ohta T, Yamakawa K, Fukushima Y, Nakamura Y, Niikawa N. Tsukamoto K, et al. Among authors: ohta t. Hum Mol Genet. 1992 Aug;1(5):315-7. doi: 10.1093/hmg/1.5.315. Hum Mol Genet. 1992. PMID: 1303207

9

Assignment of the human moesin gene (MSN) to chromosome region Xq11.2-->q12.

Kishino T, Ariga T, Soejima H, Tamura T, Ohta T, Jinno Y, Yonemura S, Sato N, Tsukita S, Tsukita S, et al. Kishino T, et al. Among authors: ohta t. Cytogenet Cell Genet. 1994;66(3):167-9. doi: 10.1159/000133692. Cytogenet Cell Genet. 1994. PMID: 8125014

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: ohta t. 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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