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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...
Autores principales: | Yue, Fagui, Jiang, Yuting, Pan, Yuan, Li, Leilei, Li, Linlin, Liu, Ruizhi, Wang, Ruixue |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614715/ https://www.ncbi.nlm.nih.gov/pubmed/31363371 http://dx.doi.org/10.3892/etm.2019.7695 |
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