The Diagnosis of Myotonic Dystrophy

McLay JS Norris A Kerr F. Could it be myotonic dystrophy. Scot Med J 1992; 37: 149–150.

Brook JD McCurrach ME Harley HG Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 1992; 68: 799–808.

Fleischer B. Uber myotonischer dystrophia mit katarakt. Albrecht von Graefes Arch Klin Ophthalmol 1918; 96: 91–133.

Koch MC Grimm T Harley HG Harper PS . Genetic risks for children of women with myotonic dystrophy. Am J Hum Genet 1991; 48: 1084–1091.

Howeler CJ Busch HFM Geraedts JPM Niermeijer MF Staal A. Anticipation in myotonic dystrophy, fact or fiction? Brain 1989; 112: 779–797.

Whitehead AS Solomon E Chambers S Bodmer WF Povey S Fey G. Assignment of the structural gene for the third component of human complement to chromosome 19. Proc Natl Acad Sci USA 1982; 79: 5021–5025.

Hunter A Tsilfidis C Mettler G Jacob P Mahadevan M Sum L Korneluk R. The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy. J Med Genet 1992; 29: 774–779.