题名 | A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion†‡ |
链接 | http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.34034/abstract;jsessionid=07869919A866F661357E75CDB429D146.f03t01 |
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