Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature

The current study presents the cases of two unrelated patients with similar clinical features, including craniofacial anomalies, developmental delay/intellectual disability and cardiac malformations, that are consistent with chromosome 10q26 deletion syndrome. High-resolution single-nucleotide polym...

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Detalles Bibliográficos
Autores principales: Lin, Shaobin, Zhou, Yi, Fang, Qun, Wu, Jianzhu, Zhang, Zhiqiang, Ji, Yuanjun, Luo, Yanmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355737/
https://www.ncbi.nlm.nih.gov/pubmed/27779662
http://dx.doi.org/10.3892/mmr.2016.5864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355737/
https://www.ncbi.nlm.nih.gov/pubmed/27779662
http://dx.doi.org/10.3892/mmr.2016.5864

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