Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs

This publication has 39 references indexed in Scilit:

• Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3
  Nature Genetics, 1996
• Preliminary phenotypic map of chromosome 4p16 based on 4p deletions
  American Journal of Medical Genetics, 1995
• Long–range mapping of gaps and telomeres with RecA–assisted restriction endonuclease (RARE) cleavage
  Nature Genetics, 1994
• Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
  Journal of Medical Genetics, 1994
• Parental origin of chromosome 4p deletion in Wolf‐Hirschhorn syndrome
  American Journal of Medical Genetics, 1993
• A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene
  Nature Genetics, 1993
• Interstitial deletion of distal chromosome 4p in a patient without classical Wolf‐Hirschhorn syndrome
  American Journal of Medical Genetics, 1993
• Molecular detection of a 4p deletion using PCR‐based polymorphisms: A technique for the rapid detection of the Wolf–Hirschhorn syndrome
  American Journal of Medical Genetics, 1992
• Nonrandom association between huntington disease and two loci separated by about 3 Mb on 4p16.3
  Genomics, 1992
• Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene
  Genomics, 1989