| Action | Exactly what to provide | Example | Why it helps |
|---|---|---|---|
| Provide key PMIDs | PMID(s) for primary EDN3/EDNRB Waardenburg–Shah / Waardenburg syndrome type IV papers | `PMID: 12345678` | Lets the next run retrieve PubMed-indexed primary literature for verifiable, PMID-linked claims |
| Provide DOI links | DOI URLs for core case reports, reviews, or mechanistic papers | `https://doi.org/10.xxxx/xxxxx` | Gives a stable article identifier when PMID retrieval is incomplete or unavailable |
| Upload PDFs | PDFs of the most important primary papers or recent reviews | `ednrb_waardenburg_shah_review.pdf` | Allows direct text extraction to create citable source contexts even if search tools fail |
| Share OMIM/Orphanet links | Direct disease/gene links for Waardenburg syndrome type IV / Waardenburg–Shah syndrome and EDN3/EDNRB | `https://omim.org/`, `https://www.orpha.net/` links | Supplies authoritative identifiers, synonyms, inheritance, and rare-disease summary fields |
| Share GeneReviews link | Link to the relevant GeneReviews chapter covering Waardenburg syndrome / syndromic Hirschsprung disease | `https://www.ncbi.nlm.nih.gov/books/` link | Provides a curated clinical synthesis for diagnostics, management, and genetic counseling |


*Table: This table lists the minimum source materials needed to unblock a fully cited EDN3/EDNRB Waardenburg–Shah report. It focuses on practical inputs—PMIDs, DOIs, PDFs, and authoritative database links—that would enable reliable evidence retrieval in a follow-up run.*