Sindrome da anomalie mammarie e degli arti OMIM 603543
Celli, J., Duijf, P., Hamel, B. C. J., et al. Heterozygous germline mutations in the p53 homolog p63 are the cause of
EEC syndrome. Cell 99: 143-153, 1999.
Guazzarotti, L., Caprio, C., Rinne, T. K.,et al. Limb-mammary syndrome (LMS)
associated with internal female genitalia dysgenesia: a new genotype/phenotype
correlation? Am. J. Med. Genet. 146A: 2001-2004, 2008.
van
Bokhoven, H., Jung, M., Smits, A. P. T., et al. Limb mammary syndrome: a new genetic disorder
with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to
human chromosome 3q27. Am. J. Hum. Genet. 64: 538-546, 1999.