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Clinical and molecular characterization of a patient with a combination of a deletion and a duplication of 22q13 using array CGH
Phelan–McDermid syndrome is caused by the loss of terminal regions of different sizes at 22q13. There is a wide range of severity of symptoms in patients with a 22q13 deletion, but these patients usually show neonatal hypotonia, global developmental delay, and dysmorphic traits. We carried out a cli...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Dove Medical Press
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3681196/ https://ncbi.nlm.nih.gov/pubmed/23776384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S35799 |
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