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Biotechnology and Genetic Engineering Reviews Volume 3, 1985 - Issue 1
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Original Articles

Myotonic Dystrophy and Gene Mapping on Human Chromosome 19

J.D. Brook Section of Medical Genetics, University of Wales College of Medicine, Heath Park, CF44XN, Cardiff, UK
,
D.J. Shaw Section of Medical Genetics, University of Wales College of Medicine, Heath Park, CF44XN, Cardiff, UK
&
A.L. Meredith Section of Medical Genetics, University of Wales College of Medicine, Heath Park, CF44XN, Cardiff, UK
Pages 311-348 | Published online: 15 Apr 2013

Citations (3)

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Read on this site (1)

Rhona G. Hughes, E. G. H. Lyall & W. A. Liston. (1991) Obstetric and neonatal complications of myotonic dystrophy. Journal of Obstetrics and Gynaecology 11:3, pages 191-194.
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Articles from other publishers (2)

Prisiliana Velázquez-Bernardino, Francisco García-Sierra, Oscar Hernández-Hernández, Mario Bermúdez de León, Geneviève Gourdon, Mário Gomes-Pereira & Bulmaro Cisneros. (2011) Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells. Molecular Biology Reports 39:1, pages 415-424.
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Anat Achiron, Yoram Barak, Nurit Magal, Moti Shohat, Maya Cohen, Rakefet Barar & Natan Gadoth. (1998) Abnormal Liver Test Results in Myotonic Dystrophy. Journal of Clinical Gastroenterology 26:4, pages 292-295.
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