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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Detalles Bibliográficos
Autores principales: Yue, Fagui, Jiang, Yuting, Pan, Yuan, Li, Leilei, Li, Linlin, Liu, Ruizhi, Wang, Ruixue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
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

Internet

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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