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REFERENCES

  • Beighton P. 1993. Heritable disorders of connective tissue. Mosby: St. Louis.
  • Celli J, Duijf P, Hamel BCJ, Bamshad M, Kramer B, Smits APT, Newbury-Ecob R, Hennekam RCM, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H. 1999. Heterozygous germline mutations in the P53 homolog of P63 are the cause of EEC syndrome. Cell 99: 143153.
  • Cervenka J. 1976. Oral and facial manifestations of cytogenetic anomalies. In: Stewart RE, editor. Prescott GH: Oral facial genetics. Mosby: St. Louis.
  • Chen RJ, Chen HS, Lin LM, Lin CC, Jorgenson RJ. 1988. Otodental dysplasia. Oral Surg 66: 353358.
  • Dianzani I, Garelli E, Gustavsson P, Carando A, Gustafsson B, Dahl N, Annerèn G. 2003. Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene. J Med Genet 40: e133.
  • Estabrook GF. 1977. Objective methods for classification and the study of birth defects. Birth Defects Orig Art Ser 13: 511.
  • Font RL, Stone MS, Schanzer MC, Lewis RA. 1986. Apocrine hidrocytomas of the lids, hypodontia, palmo-plantar hyperkeratosis, and onychodystrophy. Arch Ophthalmol 104: 18111813.
  • Freire-Maia N, Pinheiro M. 1984. Ectodermal dysplasias: A clinical and genetic study. New York: AR Liss.
  • Gorlin RJ, Cohen MM, Hennekam RCM. 1990. Syndromes of the head and neck. New York: Oxford University Press.
  • Jorgenson RJ. 1974. Ectodermal dysplasia with hypotrichosis, hypohidrosis, defective teeth and unusual dermatoglyphics (Basan syndrome?). Birth Defects Orig Art Ser 10: 323325.
  • Jorgenson RJ. 1980. A clinician's view of hypodontia. J Am Dent Assoc 101: 283286.
  • Levin LS, Jorgenson RJ, Cook RJ. 1975. Otodental dysplasia—A new ectodermal dysplasia. Clin Genet 8: 136144.
  • Opitz JM, Herrmann J, Dieker H. 1969. The study of malformation syndromes in man. Birth Defects Orig Art Ser 2: 110.
  • Pinsky L. 1975. The community of human malformation syndromes that shares ectodermal dysplasia and deformities of the hands and feet. Teratology 9: 6580.
  • Pruzansky S. 1977. Time: The fourth dimension in syndrome analysis applied to craniofacial malformations. Birth Defects Orig Art Ser 13: 328.
  • Rath JA, Duijf PHG, Doetsch V, Irvine AD, de Waal R, Vanmolkot KRJ, Wessagowit V, Kelly A, Atherton DJ, Griffiths WAD, Orlow SJ, van Haeringen A, Ausems MGEM, Yang A, McKeon F, Bamshad MA, Brunner HG, Hamel BCJ, van Bokhoven H. 2001. Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of P63. Hum Mol Genet 10: 221229.
  • Schöpf E, Schultz H-J, Passarge E. 1971. Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia, hypotrichosis as a possible autosomal recessive trait. Birth Defects Orig Art Ser 7: 219221.
  • Stewart DJ, Kinirons MJ. 1982. Globodontia. Br Dent J 152: 287288.
  • Sybert VP. 1997. Genetic skin disorders. New York: Oxford University Press.
  • Witkop CJ Jr, Gundlach KKH, Streed WJ, Sauk JJ Jr. 1976. Globodontia in the otodental syndrome. Oral Surg 41: 472483.