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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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| Publié dans: | Mol Med Rep |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
D.A. Spandidos
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5355737/ https://ncbi.nlm.nih.gov/pubmed/27779662 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2016.5864 |
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