SEARCH

SEARCH BY CITATION

REFERENCES

  • Ardinger HH. 2005. Proc Greenwood Genet Center 24: 142.
  • Braddock SR, Golabi M, Hall BD. 2008. Petty syndrome: Further delineation of a rare “old” syndrome. Presented at the 29th David W. Smith Workshop on Malformations and Morphogenesis.
  • Castori M, Silvestri E, Pedace L, Marseglia G, Tempera A, Antigoni I, Torricelli F, Majore S, Grammatico P. 2009. Fontaine–Farriaux syndrome: A recognizable craniosynostosis syndrome with nail, skeletal, abdominal, and central nervous system anomalies. Am J Med Genet Part A 149A: 21932199.
  • Delgado-Luengo WN, Petty EM, Solis-Anez E, Romel O, Delgado-Luengo J, Hernandez ML, Morales-Machin A, Borjas-Fuentes L, Zabala-Fernandez W, Gonzalez-Ferrer S, Pineda-Bernal L, Pardo-Govea T, Martinez-Basalo MC, Gonzalez R, Urdaneta K, Canizales J, Fleitas-Cabello H. 2009. Petty–Laxova–Wiedemann progeroid syndrome: Further phenotypical delineation and confirmation of a rare syndrome of premature aging. Am J Med Genet Part A 149A: 22002205.
  • Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. 2003. Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome. Nature 423: 293298.
  • Faivre L, Khau Van Kien P, Madinier-Chappat N, Nivelon-Chevallier A, Beer F, LeMerrer M. 1999. Can Hutchinson–Gilford progeria syndrome be a neonatal condition? Am J Med Genet 87: 450.
  • Fontaine G, Farriaux JP, Blanckaert D, Lefebvre C. 1977. Un nouveau syndrome polymalformatif complexe. J Genet Hum 25: 109119.
  • Myers-Benner J. 2009. Surf: For those who care for dying children. Am J Med Genet Part A 149A: 301.
  • Petty EM, Laxova R, Wiedemann H-R. 1990. Previously unrecognized congenital progeroid disorder. Am J Med Genet 35: 383387.
  • Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. 2001. Fontaine–Farriaux craniosynostosis: Second report in the literature. Am J Med Genet 100: 214218.
  • Rodriguez JI, Pérez-Alonso P, Funes R, Pérez-Rodriguez J. 1999. Lethal neonatal Hutchinson–Gilford progeria syndrome. Am J Med Genet 82: 242248.
  • Seftel MD, Wright CA, Po PLW, De Ravel TJL. 1996. Lethal neonatal mandibuloacral dysplasia. Am J Med Genet 66: 5254.
  • Wiedemann H-R. 1992. Newly recognized congenital progeriod disorder. Am J Med Genet 42: 857.
  • Yang CS, Braddock SR, Paschal BM. 2008. unpublished observations.