1. Ades, L. C., Clapton, W. K., Morphett, A., et al. (1994). Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: A new multiple malformation syndrome, or a severe form of oral–facial–digital syndrome type I. American Journal of Medical Genetics, 49, 211–217.
2. Al-Gazali, L. I., Sztriha, L., Punnose, J., et al. (1999). Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophtalmoplegia and postaxial polydactyly: A variant of orofaciodigital syndrome type VI or a new syndrome? Journal of Medical Genetics, 36, 161–166.
3. Al-Qattan, M. M., & Hassanain, J. M. A. (1997). Classification of limb anomalies in oral-facial-digital syndromes. Journal of Hand Surgery, 22B(2), 250–252.
4. Balci, S., Guler, G., Kale, G., et al. (1999). Mohr syndrome in two sisters: Prenatal diagnosis in a 22-week-old fetus with postmortem findings in both. Prenatal Diagnosis, 19, 827–831.
5. Baraitser, M. (1986). The orofaciodigital (OFD) syndromes. Journal of Medical Genetics, 23(116–119), 1986.