eScholarship
metadata only
CC BY
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development
A copy-number variant (CNV) of 16p11.2 encompassing 30 genes is associated with developmental and psychiatric disorders, head size, and body mass. The genetic mechanisms that underlie these associations are not understood. To determine the influence of 16p11.2 genes on development, we investigated t
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
- Craniofacial development: genetics, signaling pathways, teratogenic mechanisms, and clinal significance.#1097941
- Characterisation of the Novel HLA‐C*16:240 Allele by Sequencing‐Based Typing#1415133
- Pediatric critical illness endotypes reveal distinct outcomes and immune pathways shared across cause of illness#1312432
- Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization#8362
- Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of \textitHTT associated with an early disease onset in \textitC9orf72 carriers#360067
Record · ID 1424881
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