Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions

Susceptible Stages in Schwann Cells for NF1-Associated Plexiform Neurofibroma Development

(2011) L. Q. Le et al.   CANCER RESEARCH

Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989

(2011) D Gareth R Evans et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Plexiform Neurofibromas in Children with Neurofibromatosis Type 1: Frequency and Associated Clinical Deficits

(2011) Rosa Nguyen et al.   JOURNAL OF PEDIATRICS

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

(2010) Angelika C. Roehl et al.   HUMAN MUTATION

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

(2010) Eric Pasmant et al.   HUMAN MUTATION

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

(2010) V.-F. Mautner et al.   JOURNAL OF MEDICAL GENETICS

Absence of cutaneous neurofibromas in an NF1 patient with an atypical deletion partially overlapping the common 1.4 Mb microdeleted region

(2008) Hildegard Kehrer-Sawatzki et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions

(2008) Katharina Steinmann et al.   EUROPEAN JOURNAL OF HUMAN GENETICS