Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis.
第一作者:
Emma Mm,Burkitt Wright
第一单位:
Genetic Medicine Research Group, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK.
作者:
医学主题词
成年人(Adult);老年人(Aged);咖啡乳斑(Cafe-au-Lait Spots);儿童, 学龄前(Child, Preschool);女(雌)性(Female);基因, 神经纤维瘤病1型(Genes, Neurofibromatosis 1);人类(Humans);男(雄)性(Male);中年人(Middle Aged);突变(Mutation);神经纤维瘤病1型(Neurofibromatosis 1);系谱(Pedigree);脊柱疾病(Spinal Diseases)
DOI
10.1136/jmedgenet-2013-101648
PMID
23812910
发布时间
2025-05-20
基金项目
- 浏览88
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



