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  • × BMC Medical Genetic
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 全选  【符合条件的数据共：4条】

1 Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome? [期刊论文]

来源：BMC Medical Genetics

作者:Francesco Pallone;Giuseppe Novelli;Federica Sangiuolo;等

关键词:Inflammation and apoptosis of gastrointestinal mucosa;Facial dysmorphisms;...

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2 Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome? [期刊论文]

来源：BMC Medical Genetics

作者:Francesco Pallone;Giuseppe Novelli;Federica Sangiuolo;等

关键词:Inflammation and apoptosis of gastrointestinal mucosa;Facial dysmorphisms;...

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3 MECP2 duplication syndrome in a Chinese family [期刊论文]

来源：BMC Medical Genetics , 2015

作者:Yanling Yang;Xinhua Bao;Qingping Zhang;等

关键词:MECP2;Chinese family;...

使用许可:CC BY

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4 MECP2 duplication syndrome in a Chinese family [期刊论文]

来源：BMC Medical Genetics , 2015

作者:Yanling Yang;Xinhua Bao;Qingping Zhang;等

关键词:MECP2;Chinese family;...

使用许可:CC BY

预览  |  原文链接  |  全文  [ 浏览：0 下载：0  ]