Characterization of a tandemly repeated 3.3-kbKpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35

This publication has 27 references indexed in Scilit:

• Cloning and mapping of a very short (10-kb)EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)
  Muscle & Nerve, 1995
• Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystropothhy
  Human Molecular Genetics, 1994
• PAX6 mutations in aniridia
  Human Molecular Genetics, 1993
• Molecular organization and chromosomal location of human GC-rich heterochromatic blocks
  Gene, 1993
• Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
  Nature Genetics, 1992
• Pax in development
  Published by Elsevier ,1992
• An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
  Nature, 1992
• Homeobox genes and axial patterning
  Published by Elsevier ,1992
• Structure of the segmentation gene paired and the Drosophila PRD gene set as part of a gene network
  Cell, 1986
• Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
  Proceedings of the National Academy of Sciences, 1977