110 patients with at least 2 neurofibromas (331 cutaneous lesions) 11 probands fullfilled the clinical NF1 criteria 99 patients were considered sporadic (95 familial members) (absence of additional NF1-criteria). 7 of 11 probands presented NF1 germline mutations 2 NF1 patients not tested 2 NF1 proband under investigation
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