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Publications by Nicolas Parkin
Neurofibromatosis Type 1 (NF1) With an Unusually Severe Phenotype Due to Digeny for NF1 and Ryanodine Receptor 1 Associated Myopathy
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Related publications
Neurofibromatosis Type 1 (NF1)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Molecular Genetics of Neurofibromatosis Type 1 (NF1).
Journal of Medical Genetics
Genetics
Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population
Scientific Reports
Multidisciplinary
Autism Spectrum Disorder in an Unselected Cohort of Children With Neurofibromatosis Type 1 (NF1)
Journal of Autism and Developmental Disorders
Developmental
Educational Psychology
Differential MSH2 Promoter Methylation in Blood Cells of Neurofibromatosis Type 1 (NF1) Patients
European Journal of Human Genetics
Genetics
Neurofibromatosis Type 1: From Genotype to Phenotype
Journal of Medical Genetics
Genetics
Region-Specific Astrogliosis in Brains of Mice Heterozygous for Mutations in the Neurofibromatosis Type 1 (Nf1) Tumor Suppressor
Brain Research
Neuroscience
Neurology
Developmental Biology
Molecular Biology
Psychological Aspects of Von Recklinghausen Neurofibromatosis (NF1)
Journal of Medical Genetics
Genetics
Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients With Neurofibromatosis Type 1
American Journal of Human Genetics
Genetics