Neurofibromatosis I
Reference77 articles.
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. Benjamin, C. M., Colley, A., Donnai, D., et al. (1993). Neurofibromatosis type 1 (NF1): Knowledge, experience, and reproductive decisions of affected patients and families. Journal of Medical Genetics, 30, 567–574. 5. Blickstein, I., Lancet, M., & Shoham, Z. (1989). The obstetric perspective of neurofibromatosis. American Journal of Obstetrics and Gynecology, 158, 385–388, Comment in 161:501.
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