Split-hand/split-foot malformation with paternal mutation in the p63 gene

This publication has 17 references indexed in Scilit:

• Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27
  American Journal of Human Genetics, 2000
• Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome
  Cell, 1999
• Hypoplastic thymus and T-cell reduction in EECUT syndrome
  American Journal of Medical Genetics, 1997
• Genetics of split hand and split foot. A case study
  Journal of the American Podiatric Medical Association, 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
• 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
• Ectodermal Dysplasia, Ectrodactyly, and Clefting Syndrome and Bilateral Retinal Detachment
  Archives of Ophthalmology (1950), 1993
• X-Chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred
  Human Genetics, 1987
• EEC syndrome without ectrodactyly? Report of 8 cases
  Clinical Genetics, 1985