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Services were held at the Harrison and Willow Church of Christ

Individuals who have deletions of the entire NF1 gene have an increased risk of facial dysmorphism, mental retardation, early appearance of neurofibromas, and the presence of plexiform neurofibromas.1 In addition, individuals who have a specific 3 base pair in-frame deletion in exon 17 of the NF1 gene may have caf-au-lait spots, intertriginous freckling and Lisch nodules, but do not develop cutaneous, subcutaneous or plexiform neurofibromas

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The fluorescence values of the solution (Ex = 560 nm, Em = 595 nm) were measured at predetermined time points using a microplate reader (Synergy 2, BioTek Instruments Inc, USA)

May-Jun 2013;23(3):143-7

Anthony RM, MacLeay JM, Jewell DE, Brejda JJ, Gross KL