p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

This publication has 45 references indexed in Scilit:

• Split-hand/split-foot malformation with paternal mutation in the p63 gene
  Prenatal Diagnosis, 2001
• Syndromic Ectrodactyly with Severe Limb, Ectodermal, Urogenital, and Palatal Defects Maps to Chromosome 19
  American Journal of Human Genetics, 1998
• 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
• Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
  Human Molecular Genetics, 1994
• Slow Repair of Pyrimidine Dimers at p53 Mutation Hotspots in Skin Cancer
  Science, 1994
• Congenital abnormalities associated with limb deficiency defects: A population study based on cases from the Hungarian congenital malformation registry (1975–1984)
  American Journal of Medical Genetics, 1994
• 5-Methylcytosine as an Endogenous Mutagen in the Human LDL Receptor and p53 Genes
  Science, 1990
• Molecular basis of base substitution hotspots in Escherichia coli
  Nature, 1978
• The lacrimo-auriculo-dento-digital syndrome
  The Journal of Pediatrics, 1973