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Open Access
Peer-reviewed
Research Article
High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability
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Xiaohong Gong ,
Contributed equally to this work with: Xiaohong Gong, Yu-wu Jiang
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Yu-wu Jiang ,
Contributed equally to this work with: Xiaohong Gong, Yu-wu Jiang
Affiliation Department of Pediatrics, Peking University First Hospital, Beijing, China
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Xin Zhang,
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Yu An,
Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Children's Hospital of Fudan University, Shanghai, China
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Jun Zhang,
Affiliations The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China, Institute and Department of Digestive Diseases, Huashan Hospital, Fudan University, Shanghai, China
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Ye Wu,
Affiliation Department of Pediatrics, Peking University First Hospital, Beijing, China
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Jingmin Wang,
Affiliation Department of Pediatrics, Peking University First Hospital, Beijing, China
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Yangfei Sun,
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Yanyan Liu,
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Xuewu Gao,
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Yiping Shen,
Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Children's Hospital of Fudan University, Shanghai, China
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Xiru Wu,
Affiliation Department of Pediatrics, Peking University First Hospital, Beijing, China
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Zilong Qiu,
Affiliation Institute of Neuroscience, Shanghai Institute of Biological Sciences, Chinese Academy of Sciences, Shanghai, China
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Li Jin,
Affiliation The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China
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Bai-Lin Wu ,
* E-mail: wu_b@fudan.edu.cn (BW); wanghy@fudan.edu.cn (HW)
Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Children's Hospital of Fudan University, Shanghai, China
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Hongyan Wang
* E-mail: wu_b@fudan.edu.cn (BW); wanghy@fudan.edu.cn (HW)
Affiliations The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China, Institutes of Biomedical Sciences, Fudan University, Shanghai, China
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High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability
- Xiaohong Gong,
- Yu-wu Jiang,
- Xin Zhang,
- Yu An,
- Jun Zhang,
- Ye Wu,
- Jingmin Wang,
- Yangfei Sun,
- Yanyan Liu,
- Xuewu Gao
- Published: April 11, 2012
- https://doi.org/10.1371/journal.pone.0034739