Pages that link to "Q34284543"
Jump to navigation
Jump to search
The following pages link to The clinical and diagnostic implications of mosaicism in the neurofibromatoses. (Q34284543):
Displaying 50 items.
- Synchronously diagnosed pre-sacral neurofibroma and cutaneous spitzoid melanoma: a fortuitous association? (Q24795232) (← links)
- Neutrophil elastase mutations in congenital neutropenia (Q28203932) (← links)
- Quantitative assessment of whole-body tumor burden in adult patients with neurofibromatosis (Q28730289) (← links)
- Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination. (Q30358638) (← links)
- Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies. (Q30364937) (← links)
- Recurrent schwannoma postirradiation: histological review reveals mixed schwannoma and meningioma (Q30450153) (← links)
- Localized Tongue Amyloidosis in a Patient with Neurofibromatosis Type II (Q30470300) (← links)
- Hereditary Genodermatoses with Cancer Predisposition (Q30470596) (← links)
- Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas (Q30495332) (← links)
- Neurofibromatosis 1. (Q30746535) (← links)
- Multiple peripheral nerve tumors: update and review of the literature (Q30972826) (← links)
- Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome (Q33909895) (← links)
- Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis (Q34350807) (← links)
- Natural history of neurofibromatosis type 2 with onset before the age of 1 year (Q34573080) (← links)
- Neurofibromatosis 1 and neurofibromatosis 2: a twenty first century perspective. (Q34577777) (← links)
- Genetic insights into familial cancers-- update and recent discoveries (Q34783505) (← links)
- Genetics of neurofibromatosis 1 and the NF1 gene (Q34982028) (← links)
- Therapy for plexiform neurofibromas in children with neurofibromatosis 1: an overview (Q34982073) (← links)
- Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations? (Q35477813) (← links)
- Ophthalmological manifestations in segmental neurofibromatosis type 1 (Q35592549) (← links)
- Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1. (Q38636277) (← links)
- Multiple, unilateral lisch nodules in the absence of other manifestations of neurofibromatosis type 1 (Q35952925) (← links)
- Gastrointestinal manifestations of neurofibromatosis type 1 (Recklinghausen's disease): clinicopathological spectrum with pathogenetic considerations. (Q36358065) (← links)
- Mosaicism in genetic skin disorders (Q36381332) (← links)
- Guidelines for the diagnosis and management of individuals with neurofibromatosis 1 (Q36653938) (← links)
- CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids (Q36967706) (← links)
- Facial plexiform neurofibroma: is it truly just skin deep? (Q37292854) (← links)
- Cutaneous mosaicism: a molecular and clinical review (Q37405424) (← links)
- Gastrointestinal and retroperitoneal manifestations of type 1 neurofibromatosis. (Q37507736) (← links)
- Solitary oral plexiform neurofibroma: Review of literature and report of a case (Q37875552) (← links)
- Localized neurofibromatosis of the female genital system: a case report and review of the literature (Q38001159) (← links)
- Mosaic generalized neurofibromatosis 1: report of two cases (Q38227762) (← links)
- The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features (Q38248325) (← links)
- Mosaic Neurofibromatosis Type 1: A Systematic Review. (Q38580486) (← links)
- Annual review of children with neurofibromatosis type 1. (Q38612658) (← links)
- Mosaic Neurofibromatosis Type 1 in Children: A Single-Institution Experience (Q38816957) (← links)
- A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas (Q38862375) (← links)
- Prevalence of neurofibromatosis type 1 in congenital pseudarthrosis of the tibia (Q38926325) (← links)
- Segmental neurofibromatosis presenting with congenital excessive skin folds (Q42148773) (← links)
- Distinctive clinical presentation of a NF-1 patient with loss of heterozygosity of PTCH in his epithelial tumors (Q42484935) (← links)
- Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism (Q42596750) (← links)
- Plexiform neurofibroma mimicking a pancreatic cystic tumour (Q43004084) (← links)
- High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasis (Q43074046) (← links)
- Parkinson's disease: is it all in the genes? (Q45227833) (← links)
- Lentiginous mosaicism and mosaic generalized neurofibromatosis type 1. (Q45339706) (← links)
- Inherited predisposition to cancer: a historical overview. (Q46038945) (← links)
- Update on 13 Syndromes Affecting Craniofacial and Dental Structures (Q47194658) (← links)
- Clinical severity in Japanese patients with neurofibromatosis 1 based on DNB classification. (Q47227403) (← links)
- Natural course and characteristics of cutaneous neurofibromas in neurofibromatosis 1. (Q47273565) (← links)
- Presacral Multiple Cellular Schwannomas (Q47442020) (← links)