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22q13.32 Deletion and Duplication and Inversion in the Same Family: A Rare Occurrence
Chromosome 22q13.3 deletion syndrome is a well-recognized cause of global developmental delay, while duplication of the same chromosome is a rare occurrence. The presence of both abnormalities in the same family has never been reported, to our knowledge. We report a rare occurrence of 22q13.3 duplic...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
International Scholarly Research Network
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3263574/ https://ncbi.nlm.nih.gov/pubmed/22389789 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5402/2011/829825 |
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