The utility of the determination of CTG trinucleotide repeat length in hypotonic infants

Seminars in Pediatric Neurology - Tập 6 - Trang 243-246 - 1999
John B. Bodensteiner1,2,3,4, Debra L. Byler1,2,3,4, Margaret E. Jaynes1,2,3,4
1Department of Neurology, Division of Pediatric Neurology, Indiana University, Indianapolis, IN USA
2Parkersburg Neurological Associates, Parkersburg, WV USA
3Department of Neurology, West Virginia University, Morgantown, WV, USA
4Department of Pediatrics, West Virginia University, Morgantown, WV USA

Tài liệu tham khảo

Roses, 1998, Myotonic dystrophy Redman, 1993, Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring, JAMA, 269, 1960, 10.1001/jama.1993.03500150072029 Harley, 1993, Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy, Am J Hum Genet, 52, 1164 Harper, 1992, Anticipation in myotonic dystrophy: New light on an old problem, Am J Hum Genet, 51, 10
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Seminars in Pediatric Neurology

Tập 6

243-246

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