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A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
No clinical trials have been registered for holoprosencephaly 6.
6 publications have been identified in PubMed for holoprosencephaly 6. Research spans Case Report / Case Series (67%), Review / Meta-Analysis (17%), and Epidemiology / Natural History (17%).
Field NK (2026). [PMID: 41885704](https://pubmed.ncbi.nlm.nih.gov/41885704/). *J Child Neurol*. [Review / Meta-Analysis]
Keçeci R (2026). [PMID: 42125343](https://pubmed.ncbi.nlm.nih.gov/42125343/). *Mol Syndromol*. [Case Report / Case Series]
Ibold C (2025). [PMID: 41210606](https://pubmed.ncbi.nlm.nih.gov/41210606/). *Geburtshilfe Frauenheilkd*. [Epidemiology / Natural History]
Negasi Gebreslase M (2025). [PMID: 41079815](https://pubmed.ncbi.nlm.nih.gov/41079815/). *Clin Case Rep*. [Case Report / Case Series]
Xie JL (2024). [PMID: 39015932](https://pubmed.ncbi.nlm.nih.gov/39015932/). *World J Clin Cases*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Oct 4, 2026, 3:01 AM UTC
Online Mendelian Inheritance in Man