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The 3q29 Microdeletion Syndrome: Report of Three New Unrelated Patients and In Silico “RNA Binding” Analysis of the 3q29 Region
The human 3q29 microdeletion syndrome is associated with mild facial dysmorphism, developmental delay and variable congenital malformations. We report three new unrelated patients with this syndrome. We also performed in silico RNA binding analysis in silico on the 3q29 critical region genes. Severa...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2011
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3312009/ https://ncbi.nlm.nih.gov/pubmed/21626679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34080 |
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