Found 26 matching trials
Screening for Genes in Patients With Congenital Neutropenia N/A Syndromic congenital neutropenia (SCN) includes a heterogeneous group of di...
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CHU Dijon Bourgogne
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Molecular Profiling to Improve Outcome of Patients in Cancer. A Pilot Study N/A Next Generation Sequencing in cancer: a feasibility study in France to asse...
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Institut Bergonié
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Transcriptome and Metabolic Analyses of CHAPLE Disease N/A CHAPLE syndrome (complement hyperactivation, angiopathic thrombosis, protei...
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Marmara University
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Severe PID With Lymphoproliferation and Neutropenia NA The purpose of this study is to analyse the phenotype in a sub-population o...
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Service d'Immunologie Clinique et VIH - Hôpital Civil
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Cancer Genome Analysis N/A Next generation sequencing (including targeted gene seqeuncing, exome and t...
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Seoul National University Hospital
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Evaluation of the Diagnostic Contribution of High-throughput Exome Sequencing for Patients With Convulsive Encephalopathy of Unknown Etiology: Pilot Study to Improve Genetic Counselling N/A Congenital epileptic encephalopathies (EE) are predominantly genetic in ori...
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Chu Dijon Bourogne
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Study for the Multidimensional Analyses of Resistance and Toxicity to Immune- and Targeted-therapies. N/A Novel treatment modalities like targeted therapies and Immune checkpoint in...
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European Institute of oncology
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Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing NA Despite significant progress made in identification on numerous genes and g...
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CHU Amiens Picardie
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ANDDI-PRENATOME - Feasibility Study for a " Fast " Pangenomic High Throughput Sequencing Analysis in Prenatal Diagnosis N/A Prenatal diagnosis of genetic diseases is a real medical challenge. The dis...
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CHU Dijon Bourgogne
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Genetic Causes of Gestational Diabetes in the Emirati Population N/A The study aims to identify the number of MODY patients to be found among Em...
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Imperial College London Diabetes Centre
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