ClinicalTrials.gov
public full text
Public Domain
Whole Genome Trio Sequencing as a Standard Routine Test in Patients With Rare Diseases - "GENOME FIRST APPROACH"
The GENOME FIRST APPROACH project will enroll patients (n = 450) and their healthy parents with unclear molecular cause of the disease, suspected genetic cause of the disease and the healthy parents of those affected for trio analysis (N in total 1350).
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Population Genomic Diversity of France#827441
- Stratified evaluation of blood RNA sequencing in a rare disease cohort#318528
- Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.#866227
- Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations#976461
- PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read Sequencing#827963
Record · ID 993345
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive