44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies: 19–21 July 1996, Naarden, The Netherlands

This publication has 7 references indexed in Scilit:

• Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1
  Human Molecular Genetics, 1996
• Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).
  Journal of Medical Genetics, 1996
• Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35
  Human Molecular Genetics, 1996
• Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
  Human Molecular Genetics, 1995
• The FSHD-linked locus D4F104S1 (p13E-11) ON 4q35 has a homologue on 10qter
  Muscle & Nerve, 1995
• A scapular onset muscular dystrophy without facial involvement: Possible allelism with facioscapulohumeral muscular dystrophy
  Neuromuscular Disorders, 1994
• FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
  Human Molecular Genetics, 1993