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Genetic Risk Factors of the Sneddon Syndrome N/A Sneddon syndrome (SS) is a rare disorder with an incidence of about 4/milli...
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Karl Landsteiner University
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Motor Impairments in Children With Autism Spectrum Disorder: a Multimodal Approach NA The general goal of the present proposal, Progetto MOSAICO, is the identifi...
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Aortic Dilatation Under 5 cm: Genetic Risk Mapping N/A This retrospective study investigates the prevalence of genetic mutations i...
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Samsun University Faculty of Medicine
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Parallel Sequencing of Fetal Genome and RNA in the Presence of Ultrasound Warning Signs: a Complementary Approach for the Prenatal Diagnosis of Rare Diseases. N/A Prenatal exome sequencing (ES) is increasingly used for fetuses with ultras...
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Hôpital Necker Enfants malades
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Male breAsT cAncer preDisposition Factor: Creation of a Control Cohort 2 NA This is an interventional, prospective, single-center study designed to col...
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Institut Universitaire du Cancer Toulouse - Oncopole, Laboratoire d'oncogénétique
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Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks NA Pathogenic variants in subcortical maternal complex (SCMC) have been identi...
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Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
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Multi-omics Study on the Pathogenesis of Malignant Transformation of Adenomyosis N/A This study is to explore the driving genes and the molecular mechanism of m...
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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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Assessment of the TGF-beta Pathway and Micro-RNA in Pediatric Pulmonary Arterial Hypertension N/A This is a prospective pilot study to assess the plasma levels of particular...
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Children's Hospital of Wisconsin
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Search for New Genetic Mutations Major Effect in Crohn's Disease N/A This study highlight genetics mutations with major effect in Crohn's Diseas...
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CHRU, Hôpital Claude Huriez
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