1. American Academy of Pediatrics Committee on Genetics. (1995). Health supervision for children with neurofibromatosis. Pediatrics, 96, 368–372.
2. Ars, E., Kruyer, H., Gaona, A., et al. (1999). Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation. Prenatal Diagnosis, 19, 739–742.
3. Barker, D., Wright, E., Nguyen, K., et al. (1987). Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. Science, 236, 1100–1102.
4. Blickstein, I., Lancet, M., & Shoham, Z. (1988). The obstetric perspective of neurofibromatosis. American Journal of Obstetrics and Gynecology, 158, 385–388. Comment in 161:501.
5. Boyd, K. P., Korf, B. R., & Theos, A. (2009). Neurofibromatosis type 1. Journal of the American Academy of Dermatology, 61, 1–16.