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A Rare Novel Copy Number Variation of Xp22.33-p11.22 Duplication is Associated with Congenital Heart Defects
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| Publicat a: | Chin Med J (Engl) |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4736901/ https://ncbi.nlm.nih.gov/pubmed/26481757 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.167369 |
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