Li H, Yamagata T, Mori M, Momoi MY: "Association of autism in two patients with hereditary multiple exostoses that is caused by the novel deletion mutations of EXT1"Journal of Human Genetics. (in press). (2002)
Li H, Yamagata T, Mori M, Momoi MY: "Association of autism in two patients with hereditary multiple exostoses that is caused by the novel deletion mutations of EXT1"Journal of Human Genetics. (in press). (2002)
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Li H、Yamagata T、Mori M、Momoi MY:“两名患有遗传性多发性外生骨疣的患者与由 EXT1 的新型缺失突变引起的自闭症相关”《人类遗传学杂志》。
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