טוען...
Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman
BACKGROUND: The 18p terminal deletion with inverted duplication is an extremely rare chromosome structure abnormality and the common clinical manifestations include intellectual disability and speech delay, etc. Up to now, only three confirmed cases were reported in Europe, and here, for the first t...
שמור ב:
| הוצא לאור ב: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732341/ https://ncbi.nlm.nih.gov/pubmed/31317671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.868 |
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