Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27

This publication has 25 references indexed in Scilit:

• A Novel Human Gene Encoding an F-box/WD40 Containing Protein Maps in the SHFM3 Critical Region on 10q24
  Biochemical and Biophysical Research Communications, 1999
• Fine Mapping of the Split-Hand/Split-Foot Locus (SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion
  American Journal of Human Genetics, 1999
• Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.
  Journal of Medical Genetics, 1996
• Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
  Human Molecular Genetics, 1996
• The EEC syndrome: a literature study
  Clinical Dysmorphology, 1996
• MOLMOL: A program for display and analysis of macromolecular structures
  Journal of Molecular Graphics, 1996
• Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: Further evidence for the existence of a limb defect gene in 6q21
  American Journal of Medical Genetics, 1995
• Deletion of chromosome 2q24‐q31 causes characteristic digital anomalies: Case report and review
  American Journal of Medical Genetics, 1995
• Crystal Structure of a p53 Tumor Suppressor-DNA Complex: Understanding Tumorigenic Mutations
  Science, 1994
• The DNA-binding domain of p53 contains the four conserved regions and the major mutation hot spots.
  Genes & Development, 1993