Article
Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature.
Molecular medicine reports - 1 Dec 2016
Lin Shaobin, Zhou Yi, Fang Qun, Wu Jianzhu, Zhang Zhiqiang, Ji Yuanjun, Luo Yanmin
Abstract excerpt
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 polymorphism analysis revealed that 10q26 terminal deletions were present in these two patients. The locations and sizes...
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