NL-OMON40473已完成不适用
sing next generation sequencing to find causative genes in patients with epidermolysis bullosa - NextGen4EB
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 2 至 99(—)
入选标准
- •-Clinically diagnosed EB or fmaily member of EB patient
- •-Antigen mapping and/or electron microscopy of a skin biopsy confirming the diagnosis of EB.
- •-No known mutation in one of the EB genes.
- •-Signed Informed consent
排除标准
- •Lack of informed consent
研究者
相似试验
已完成
不适用
sing next generation sequencing to find causative genes in patients with severe microcephalymicrocephalyNL-OMON35505niversitair Medisch Centrum Groningen750
进行中(未招募)
不适用
ext Generation Sequencing and Induced Pluripotent Stem Cell Applications in Genetic and Inheritable Forms of Renal DiseaseACTRN12615000140550Genetic Health Queensland, RBWH236
已完成
不适用
Sequencing in Suspected Infection (SePSI)ndiagnosed undifferentiated febrile illness in adultsSigns and SymptomsISRCTN11747901niversity Hospital Southampton NHS Foundation Trust (UK)100
已完成
1 期
tilizing Next Generation Sequencing to Evaluate Genomic Complexity in Thai Patients with Multiple MyelomaThe newly diagnose with MMThe newly diagnose with plasma cell disorderRelapse MM patientThai populationNext Generation SequencingSomatic mutationMultiple MyelomaTCTR20211020003/A27
招募中
不适用
Whole exome sequencing to unravel the genetics of neuralgic amyotrophyNL-OMON41857eurologie250
