טוען...
Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1
The subchromosomal region 1q21.1 is one of the hotspots in the human genome for deletions and reciprocal duplications, owing to the existence of hundreds of segmental duplications. Recurrent deletions and duplications in this region are thought to be causative in patients with variable clinical mani...
שמור ב:
| הוצא לאור ב: | Front Genet |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Media S.A.
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7325322/ https://ncbi.nlm.nih.gov/pubmed/32655619 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00577 |
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