Associated Papers
Neurofibromatosis: novel and recurrent mutations in Turkish patients.
Terzi YK et al.
Pediatric Neurology, 2007
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1.
Girodon-Boulandet E et al.
Human Mutation, 2000
Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers.
Oğuzkan S et al.
The Turkish Journal of Pediatrics, 0
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