New publication
Genes & inheritance
1 supporting source
confidence 97%
novelty 75%
Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities
To evaluate the clinical utility of genetic testing via karyotyping, chromosomal microarray analysis (CMA), and exome sequencing in cases with corpus callosum abnormalities (CCA).
How this was derived
Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).
Generated 2026-11-13, last changed
yesterday. Dedup key newdoc:366.
The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.
Evidence (1 quote)
Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities
peer_reviewed
· published 2025-01-01
· live page
Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.
Supporting documents (1)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| Prenatally and postnatally sequential genetic etiology detection in... | pmc | 2025-01-01 | yesterday | 1.00 |