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Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
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| 2019 | 1 |
| 2026 | 1 |
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Page 1
Lathosterolosis: An Extremely Rare Inherited Condition Associated With Progressive Liver Disease.
J Pediatr Gastroenterol Nutr. 2019 Nov;69(5):e142-e145. doi: 10.1097/MPG.0000000000002434.
J Pediatr Gastroenterol Nutr. 2019.
PMID: 31259789
No abstract available.
Choroidal melanoma and polydactylous onychopapilloma leading to diagnosis of BAP1 tumor predisposition syndrome.
Miano DI, Ferguson E, Oswalt C, Materin MA.
Miano DI, et al. Among authors: ferguson e.
Ophthalmic Genet. 2026 Jul 2:1-3. doi: 10.1080/13816810.2026.2697757. Online ahead of print.
Ophthalmic Genet. 2026.
PMID: 42394126
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