REFERENCES
- Battaglia A., Orsitto E., Gibilisco G. Mental retardation, epilepsy, short stature, and skeletal dysplasia: confirmation of the Gurrieri syndrome. Am J Med Genet 1996; 62: 230–232
- Coffin G. S., Siris E., Wegienka L. C. Mental retardation with osteocartilagineous anomalies. Am J Dis Child 1966; 112: 205
- Fleck B. J., Pandya A., Vanner L, Kerkering K, Bodurtha J. Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. Am J Med Genet 2001; 99: 1–7
- Garcias G. L., Martino-Roth M. G., Schuch C. Hx˙ Mx˙ V. Retardo Mental, Fácies Grosseira e Andar Simiesco. Uma nova Síndrome?. XLIII Encontro Anual da SBPC. 1991; 14(1): 32
- Hunter A.G. W. Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes. Am J Med Genet 2002; 111: 345–355
- Lowry R. B., Miller J R, Fraser F C. A new dominant gene mental retardation sysdrome: associated with small stature, tapering fingers, characteristic facies, and possible hydrocephalus. Am J Dis Child 1971; 121: 496–500
- Mattei J F, Laframboise R, Rouault F, Giraud F. Coffin-Lowry syndrome in sibs. Am J Med Genet 1981; 8: 315–320
- Online Mendelian Inheritance in Man, OMIM, (TM). McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD). 2000
- Tan U. A new syndrome with quadrupedal gait, primitive speech, and severe mental retardation as a live model for human evolution. Int J Neurosc 2006; 116: 361–369
- Winter R M, Baraitser M. The London Dysmorphology Database: A Computerised Database for the Diagnosis of Rare Dysmorphic Syndromes: version 3. Oxford University Press. 2003