Heterozygous Deletion on Chromosome 2p21 Causes a Newly Recognized Syndrome Comprising Conductive He

来源 :第十四次全国医学遗传学学术会议 | 被引量 : 0次 | 上传用户:fred20099
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  Objective: To report clinical characterization and identify molecular cytogenetic characterization of a newly syndrome for conductive hearing loss with ptosis in an autosomal dominant inheritance family.
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