The FSHD-linked locus D4F104S1 (p13E-11) ON 4q35 has a homologue on 10qter

This publication has 9 references indexed in Scilit:

• Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
  Published by Elsevier ,2004
• Pulsed-Field Gel Electrophoresis of the D4F104S1 Locus Reveals the Size and the Parental Origin of the Facioscapulohumeral Muscular Dystrophy (FSHD)-Associated Deletions
  Genomics, 1994
• Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11
  Human Molecular Genetics, 1993
• Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements
  Human Molecular Genetics, 1993
• Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events
  Nature Genetics, 1993
• No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers
  Human Molecular Genetics, 1993
• FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
  Human Molecular Genetics, 1993
• Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
  Nature Genetics, 1992
• Genomic sequencing.
  Proceedings of the National Academy of Sciences, 1984