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Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report
Trisomy 16q is a rare disorder with severe abnormalities, which always leads to early postnatal mortality. It usually results from a parental translocation, exhibiting 16q duplication associated with another chromosomal deletion. The present study reports on the clinical presentation and molecular c...
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| Gepubliceerd in: | Exp Ther Med |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
D.A. Spandidos
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6614715/ https://ncbi.nlm.nih.gov/pubmed/31363371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2019.7695 |
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