Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference24 articles.
1. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy;Bodrug;Science,1987
2. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy;Boyd;Clin. Genet,1986
3. Muscular dystrophy in girls with X; autosome translocations;Boyd;J. Med. Genet,1986
4. Mapping of twelve Xp21 translocation breakpoints with respect to the locus for Duchenne muscular dystrophy;Boyd;Cytogenet. Cell Genet,1988
5. Molecular heterogeneity of translocations associated with muscular dystrophy;Boyd;Clin. Genet,1987
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1. The Evolution of an Intron: Analysis of a Long, Deletion-Prone Intron in the Human Dystrophin Gene;Genomics;1997-03
2. Molecular characterization of further dystrophin gene microsatellites;Molecular and Cellular Probes;1995-10
3. Mapping of 386 kb of genomic DNA in the human dystrophin-encoding gene (DYS) using an ordered phage λ sublibrary of a YAC clone containing the DYS region;Gene;1994-01
4. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome;American Journal of Medical Genetics;1993-11-15
5. Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.;Journal of Medical Genetics;1993-09-01
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