X chromosomal deletion due to microhomology-mediated break-induced replication in a boy with Xp22.3 contiguous gene deletion syndrome: Implications for novel genomic defects leading to Kallmann Syndrome.
X chromosomal deletion due to microhomology-mediated break-induced replication in a boy with Xp22.3 contiguous gene deletion syndrome: Implications for novel genomic defects leading to Kallmann Syndrome.
复制标题
患有 Xp22.3 连续基因缺失综合征的男孩因微同源介导的断裂诱导复制而导致 X 染色体缺失：对导致卡尔曼综合征的新型基因组缺陷的影响。
DOI：
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发表时间：
2016
期刊：
影响因子：
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通讯作者：
Fukami M.
中科院分区：
文献类型：
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作者：
Nagai K;Shima H;Kamimura M;Kanno J;Fujiwara I;Suzuki E;Narumi S;Ishiguro A;Fukami M.
