A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity
about
Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in FranceWatson syndrome: is it a subtype of type 1 neurofibromatosis?Molecular genetics of neurofibromatosis type 1 (NF1)The neurofibromatosis type I messenger RNA undergoes base-modification RNA editingEffect of simvastatin on cognitive functioning in children with neurofibromatosis type 1: a randomized controlled trialNeurology and the skin.The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.Malignant peripheral nerve sheath tumours in neurofibromatosis 1A potential role for NF1 mRNA editing in the pathogenesis of NF1 tumorsA RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressorMAPK pathway activation in pilocytic astrocytomaThe Nf1 tumor suppressor regulates mouse skin wound healing, fibroblast proliferation, and collagen deposited by fibroblastsRegion-specific astrogliosis in brains of mice heterozygous for mutations in the neurofibromatosis type 1 (Nf1) tumor suppressorNeurofibromatosis Type 1 Presenting with Ophthalmic Features: A Case SeriesOptimizing biologically targeted clinical trials for neurofibromatosis.Growth in North American white children with neurofibromatosis 1 (NF1)Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromesMortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989.Mortality associated with neurofibromatosis type 1: a study based on Italian death certificates (1995-2006)A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.Segregation analysis of peripheral neurofibromatosis (NF1)A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counsellingTumor-suppressor genes: cardinal factors in inherited predisposition to human cancersEpilepsy in individuals with neurofibromatosis type 1.Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1.Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism.A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.Neurofibromatosis type 1 in Israel: survey of young adults.Von Hippel-Lindau disease: a genetic study.A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkageMales with familial idiopathic scoliosis: a distinct phenotypic subgroupAscertainment and severity of Marfan syndrome in a Scottish population.Leukaemia and Sellafield: is there a heritable link?Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.Minor disease features in neurofibromatosis type 1 (NF1) and their possible value in diagnosis of NF1 in children < or = 6 years and clinically suspected of having NF1. Neurofibromatosis team of Sophia Children's HospitalCharacterisation of germline mutations in the neurofibromatosis type 1 (NF1) geneGenetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.The NF1 somatic mutational landscape in sporadic human cancers.Three independent mutations in the TSC2 gene in a family with tuberous sclerosis.Elevated risk for MPNST in NF1 microdeletion patients.
P2860
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P2860
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity
description
1989 nî lūn-bûn
@nan
1989 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
A genetic study of von Recklin ...... ental transmission on severity
@ast
A genetic study of von Recklin ...... ental transmission on severity
@en
A genetic study of von Recklin ...... ental transmission on severity
@en-gb
A genetic study of von Recklin ...... ental transmission on severity
@nl
type
label
A genetic study of von Recklin ...... ental transmission on severity
@ast
A genetic study of von Recklin ...... ental transmission on severity
@en
A genetic study of von Recklin ...... ental transmission on severity
@en-gb
A genetic study of von Recklin ...... ental transmission on severity
@nl
prefLabel
A genetic study of von Recklin ...... ental transmission on severity
@ast
A genetic study of von Recklin ...... ental transmission on severity
@en
A genetic study of von Recklin ...... ental transmission on severity
@en-gb
A genetic study of von Recklin ...... ental transmission on severity
@nl
P2093
P2860
P3181
P356
P1476
A genetic study of von Recklin ...... ental transmission on severity
@en
P2093
P2860
P304
P3181
P356
10.1136/JMG.26.11.704
P407
P577
1989-11-01T00:00:00Z