Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers-Reference-Cited by-同舟云学术

Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers

Published:1989-09 Issue:3 Volume:34 Page:189-194
ISSN:0021-5074
Container-title:Japanese journal of human genetics
language:en
Short-container-title:Jap J Human Genet

Author:

Takemoto Yuji,Miki Tetsuro,Nakura Jun,Nishikawa Kumi,Kamino Kouzin,Takeda Shunichi,Kuzu Kogo,Osame Mitsuhiro,Nakagawa Masanori,Higuchi Itsuro,Yamada Takeshi,Takayanagi Tetsuya,Matsubara Shiro,Saita Kyoko,Takai Shin-ichiro,Honjo Tasuku,Ogihara Toshio

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/jhg198914.pdf

Reference13 articles.

1. Bartlett, R.J., Pericak-Vance, M.A., Yamaoka, L., Gilbert, J., Herbstreith, M., Hung, W.-Y., Lee, J.E., Mohandas, T., Bruns, G., Laberge, C., Thibault, M.-C., Ross, D. and Roses, A.D. 1987. A new probe for the diagnosis of myotonic muscular dystrophy.Science 235: 1648–1650.

2. Griggs, R., Wood, D., Moxley, R., Ashizawa, T., Epstein, H., Hejtmancik, F., Bartllet, R., Gilbert, J., Lee, J., Pericak-Vance, M., Roses, A., Brook, J., Howell, R., Johnson, K., Junien, C., Korneluk, R., Mohrenweiser, H., Ropers, H-H., Shaw, D., Siciliano, M. and Todd, J. 1989. Criteria for establishing the validity of genetic recombination in myotonic dystrophy.Neurology 39: 420–421.

3. Johnson, K., Nimmo, E., Jones, P., Weiss, M., Savontaus, M.-L., Anvret, M., Bartlett, R., Roses, A., Shaw, D., Harper, P.S., Koivunen-Tapio, E. and Williamson, R. 1988. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.Hum. Genet. 80: 379–381.

4. Lunt, P.W., Meredith, A.L. and Harper, P.S. 1986. First-trimester prediction in fetus at risk for myotonic dystrophy.Lancet II: 350–351.

5. Meredith, A.L., Huson, S.M., Lunt, P.W., Sarfarazi, M., Harley, H.G., Brook, J.D. and Harper, P.S. 1986. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.Br. Med. J. 293: 1353–1356.