An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy-Reference-Cited by-同舟云学术

An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

Published:1992-03-06 Issue:5049 Volume:255 Page:1256-1258
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Fu Y. H.¹,Pizzuti A.¹,Fenwick R. G.¹,King J.²,Rajnarayan S.¹,Dunne P. W.³,Dubel J.³,Nasser G. A.³,Ashizawa T.³,de Jong P.⁴,Wieringa B.⁵,Korneluk R.⁶,Perryman M. B.⁷,Epstein H. F.³,Caskey C. Thomas²

Affiliation:

1. Institute for Molecular Genetics, Baylor College of Medicine, Houston, TX 77030.

2. Institute for Molecular Genetics and Human Genome Center, Baylor College of Medicine, Houston, TX 77030.

3. Department of Neurology, Baylor College of Medicine, Houston, TX 77030.

4. Lawrence Livermore Laboratory, University of California, Livermore, CA 94550.

5. Department of Cell Biology and Histology, University of Nijmegen, Nijmegen, The Netherlands.

6. Department of Genetics, Children's Hospital, Eastern Ontario, Canada.

7. Department of Cardiology, Baylor College of Medicine, Houston, TX 77030.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference21 articles.

1. ASLANIDIS, C, CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT, NATURE 355: 548 (1992).

2. EDWARDS, A, DNA TYPING AND GENETIC-MAPPING WITH TRIMERIC AND TETRAMERIC TANDEM REPEATS, AMERICAN JOURNAL OF HUMAN GENETICS 49: 746 (1991).

3. FU, Y.H., VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX, CELL 67: 1047 (1991).

4. GIBBS, R.A., MULTIPLEX DNA DELETION DETECTION AND EXON SEQUENCING OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE GENE IN LESCH-NYHAN FAMILIES, GENOMICS 7: 235 (1990).

5. Goldstein, J. L., Metabolic Basis of Inherited Disease: CH48 (1989).

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