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Identification of a 17p13.3 microdeletion in a family with metal retardation and developmental delay
[会议论文] 作者：YANGYing[1]LIJie[1]ZHURui-fang[1]ZHUXiang-yu[1]HELin-lin[1]WangWan-jun[1]WANGYa-ping[2]HUYa-li;,
来源：江苏省第九次围产医学会议 年份：2013
We report on a familial case of small 17p13.3 chromosomal deletion.Conventional karyotyping revealed a der(17) in a family.HumanCytoSNP-12 Chip analysis ide...
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