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Cloning of the essential myotonic dystrophy region and mapping of the putative defect

Author

Gert Jansen

Published in: Nature

Date of publication: February 1, 1992

Language: English

Main subject: myotonic dystrophy, molecular cloning

Bibliographic databases:

Cites articles 14

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Authors

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Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors
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A high-resolution, fluorescence-based, semiautomated method for DNA fingerprinting
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Criteria for establishing the validity of genetic recombination in myotonic dystrophy
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Optimizing restriction fragment fingerprinting methods for ordering large genomic libraries
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Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locus
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Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy
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Mspl RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112)
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A frequent Hincll polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118)
March 1, 1991

A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119)
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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
May 1, 1991

Fragile X genotype characterized by an unstable region of DNA.
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Identification of new DNA markers close to the myotonic dystrophy locus
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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
February 1, 1992

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

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