1. Jones KL. Oral-facial-digital syndrome. In: Jones KL. Smith´s Recognizable Patterns of Human Malformation. 5th ed. Philadelphia: Saunders, 1997: 262-3.

2. Franceschini P, Guala A, Vardeu M, Signorile F, Franceschini D, Bolgiani M. Short rib dysplasia group (with/without polydactily): Report of a patient suggesting the existence of a continuous spectrum. Am J Med Genet 1995; 59(3): 359-64.

3. Leao M, Ribeiro-Silva M. Oral-facial-digital Syndrome type I in a patient with severe CNS defects. Pediatr Neurol 1995; 13(3): 247-51.

4. Orstavik K, Tangsrud S, Nordshus T, Finnanger A, Hellurn C, Gjessing E. Oral-facial-digital Syndrome type I in a girl with unilateral tibial pseudarthrosis. J Med Genet 1992; 29(11): 827-30.

5. Odent S, Le Marec B, Toutain A, Vigneron J, Treguier C, et al. Central nervous system malformations and early end-stage renal disease in Oral-facial-digital Syndrome type I: A review. Am J Med Genet 1998; 75(4): 389-94.

6. Jones KL. Mohr Syndrome. In: Jones KL. Smith´s Recognizable patterns of Human Malformation. 5th Ed. Philadelphia: Saunders, 1997: 264-5.

7. Reardon W, Harboro M, Hall-Craggs M, Kendall B, Brett E, Baraitser M. Central nervous system malformations in Mohr´s Syndrome. J Med Genet 1989; 26: 659-63.

8. Prpic I, Cekada S, Franulovic J. Mohr Syndrome (oral-facial-digital syndrome II) – A familiar case with different phenotypic findings. Clin Genet 1995; 48(6): 304-7.