Ontology highlight
ABSTRACT:
SUBMITTER: Lin S
PROVIDER: S-EPMC5355737 | biostudies-literature | 2016 Dec
REPOSITORIES: biostudies-literature
Lin Shaobin S Zhou Yi Y Fang Qun Q Wu Jianzhu J Zhang Zhiqiang Z Ji Yuanjun Y Luo Yanmin Y
Molecular medicine reports 20161019 6
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 of the 10q26 deletions in these two patients were compared with the locations and si ...[more]