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Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.
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Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
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The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
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The use of apolipoprotein CII as a genetic marker for myotonic dystrophy.
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Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.
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Myotonic dystrophy: opportunities for prenatal prediction.
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Cognitive behaviour therapy plus aerobic exercise training to increase activity in patients with myotonic dystrophy type 1 (DM1) compared to usual care (OPTIMISTIC): study protocol for randomised controlled trial.
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Cataract and myotonic dystrophy: the role of molecular diagnosis.
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3
Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.
J Med Genet. 1991 Feb;28(2):89-91. doi: 10.1136/jmg.28.2.89.
4
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.
J Med Genet. 1992 Nov;29(11):785-8. doi: 10.1136/jmg.29.11.785.
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Minimal expression of myotonic dystrophy: a clinical and molecular analysis.
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本文引用的文献
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Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
Clin Genet. 1983 Sep;24(3):159-70. doi: 10.1111/j.1399-0004.1983.tb02233.x.
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The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.
Hum Genet. 1984;68(4):286-9. doi: 10.1007/BF00292585.
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Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci.
Am J Hum Genet. 1972 May;24(3):310-6.
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The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
Hum Genet. 1985;70(3):271-3. doi: 10.1007/BF00273455.
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Criteria for establishing the validity of genetic recombination in myotonic dystrophy.
Neurology. 1989 Mar;39(3):420-1. doi: 10.1212/wnl.39.3.420.
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Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
Br Med J (Clin Res Ed). 1986 Nov 22;293(6558):1353-6. doi: 10.1136/bmj.293.6558.1353.
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First-trimester prediction in fetus at risk for myotonic dystrophy.
Lancet. 1986 Aug 9;2(8502):350-1. doi: 10.1016/s0140-6736(86)90044-9.
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Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).
Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680.
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A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.
Genomics. 1989 Feb;4(2):146-51. doi: 10.1016/0888-7543(89)90293-0.
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Congenital myotonic dystrophy in Britain. II. Genetic basis.
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