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Chromosomal disorder in which chromosome 13 is affected.
Biomarker and diagnostic research for chromosome 13 disorder has been reported in the published literature.
No clinical trials have been registered for chromosome 13 disorder.
44 publications have been identified in PubMed for chromosome 13 disorder. Research spans Case Report / Case Series (39%), Epidemiology / Natural History (27%), and Basic Science / Preclinical (25%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 17 | 39% |
Data assembled from 2 of 12 sources · Last updated Sep 21, 2026, 11:06 AM UTC
12 |
27% |
Laboratory research | 11 | 25% |
Research summaries | 2 | 5% |
Testing and diagnosis research | 1 | 2% |
New treatment approaches | 1 | 2% |
Zamarro Díaz LÁ (2026). [PMID: 41714141](https://pubmed.ncbi.nlm.nih.gov/41714141/). *Pediatric dermatology*. [Case Report / Case Series]
Zhong J (2026). [PMID: 42100385](https://pubmed.ncbi.nlm.nih.gov/42100385/). *Front Oncol*. [Case Report / Case Series]
Kato N (2026). [PMID: 40974038](https://pubmed.ncbi.nlm.nih.gov/40974038/). *American journal of medical genetics. Part A*. [Epidemiology / Natural History]
Gao JF (2026). [PMID: 40921432](https://pubmed.ncbi.nlm.nih.gov/40921432/). *Clinical genetics*. [Basic Science / Preclinical]
Qi Y (2026). [PMID: 42221008](https://pubmed.ncbi.nlm.nih.gov/42221008/). *Front Pediatr*. [Case Report / Case Series]
Pan Q (2025). [PMID: 39843573](https://pubmed.ncbi.nlm.nih.gov/39843573/). *Scientific reports*. [Epidemiology / Natural History]
Pei Y (2025). [PMID: 41233895](https://pubmed.ncbi.nlm.nih.gov/41233895/). *Genome medicine*. [Basic Science / Preclinical]
Drallmeier M (2025). [PMID: 40385890](https://pubmed.ncbi.nlm.nih.gov/40385890/). *Cureus*. [Epidemiology / Natural History]
He D (2025). [PMID: 40076727](https://pubmed.ncbi.nlm.nih.gov/40076727/). *International journal of molecular sciences*. [Basic Science / Preclinical]
Chevallier L (2025). [PMID: 40131457](https://pubmed.ncbi.nlm.nih.gov/40131457/). *Mammalian genome : official journal of the International Mammalian Genome Society*. [Case Report / Case Series]