Assignment of the dentatorubral and pallidoluysian atrophy (DRPLA) gene to 12p13.31 by fluorescence in situ hybridization

Genomics

Volumn 32, Issue 1, 1996, Pages 171-172

  Takano, Takako ^a   Yamanouchi, Yasuko ^a   Nagafuchi, Shigeo ^b   Yamada, Masao ^b  

^a TEIKYO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; TRINUCLEOTIDE;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 12P; CHROMOSOME R BAND; CLINICAL FEATURE; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DNA NICK TRANSLATION; DNA PROBE; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ASSIGNMENT; HUMAN; HUMAN CELL; LYMPHOCYTE CULTURE; MALE; METAPHASE CHROMOSOME; NUCLEOTIDE REPEAT; PRIORITY JOURNAL;

EID: 0029993351     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0100     Document Type: Article

References (7)

1. ISCN (1985). An international system for human cytogenetic nomenclature. Cytogenet. Cell Genet. 35: 54.
2. Koide, R., Ikeuchi, T., Onodera, O., Tanaka, H., Igarashi, S., Endo, K., Takahashi, H., Kondo, R., Ishikawa, A., Hayashi, T., Saito, M., Tomoda, A., Miike, T., Naito, H., Ikuta, F., and Tsuji, S. (1994). Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet. 6: 9-13.
3. Nagafuchi, S., Yanagisawa, H., Sato, K., Shirayama, T., Ohsaki, E., Bundo, M., Takeda, T., Tadokoro, K., Kondo, I., Murayama, N., Tanaka, Y., Kikushima, H., Umino, K., Kurosawa, H., Furukawa, T., Nihei, K., Inoue, T., Sano, A., Komure, O., Takahashi, M., Yoshizawa, T., Kanazawa, I., and Yamada, M. (1994). Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nature Genet. 6: 14-18.
4. Nagafuchi, S., Yanagisawa, H., Ohsaki, E., Shirayama, T., Tadokoro, K., Inoue, T., and Yamada, M. (1994). Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA). Nature Genet. 8: 177-182.
5. Takahashi, E-I., Hori, T., O'Connell, P., Leppert, M., and White, R. (1990). R-banding and nonisotopic in situ hybridization: Precise localization of the human type II collagen gene (COL2A1). Hum. Genet. 86: 14-16.
6. Takahashi, E-I., Hori, T., and Sutherland, G. R. (1990). Mapping of the human type II collagen gene (COL2A1) proximal to fra(12)(q13.1) by nonisotopic in situ hybridization. Cytogenet. Cell Genet. 54: 84-85.
7. Takahashi, E-I., Yamauchi, M., Tsuji, H., Hitomi, A., Meuth, M., and Hori, T. (1991). Chromosome mapping of the human cytidine-5′-triphosphate synthetase (CTPS) gene to band 1p34.1-p34.3 by fluorescence in situ hybridization. Hum. Genet. 88: 119-121.