Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q
- 1 January 1995
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 18 (S13) , S98-S102
- https://doi.org/10.1002/mus.880181318
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystropothhyHuman Molecular Genetics, 1994
- FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitHuman Molecular Genetics, 1993
- Genetic and physical maps of human chromosome 4 based on dinucleotide repeatsGenomics, 1992
- Diagnostic criteria for facioscapulohumeral muscular dystrophyNeuromuscular Disorders, 1991
- Hearing loss in facioscapulohumeral muscular dystrophyNeurology, 1991
- Gene structure and chromosomal localization of plasma kallikreinBiochemistry, 1991
- Genetic maps of mouse Chromosome 17 including 12 new anonymous DNA loci and 25 anchor lociGenomics, 1991
- Mouse Plasma Kallikrein: cDNA Structure, Enzyme Characterization, and Comparison of Protein and mRNA Levels among SpeciesDNA and Cell Biology, 1990
- Location of facioscapulohumeral muscular dystrophy gene on chromosome 4The Lancet, 1990
- Hearing loss in facioscapulohumeral dystrophyEuropean Journal of Pediatrics, 1986