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Mutations in MSH5 in Primary Ovarian Insufficiency 期刊论文
Human Molecular Genetics, 2017, 卷号: 26, 期号: 8, 页码: 1452-1457
Authors:  Ting Guo;  Shi-Dou Zhao;  Shi-Gang Zhao;  Chen M(陈敏);  Guang-Yu Li;  Xue Jiao;  Zhao Wang;  Yue-Ran Zhao;  Qin YY(秦莹莹);  Gao F(高飞);  Chen ZJ(陈子江)
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CRISPR/Cas9-Mediated Dax1 Knockout in the Monkey Recapitulates Human AHC-HH 期刊论文
Human Molecular Genetics, 2015, 卷号: 24, 期号: 25, 页码: 7255-7264
Authors:  Yu Kang;  Bo Zheng;  Bin Shen;  Yong-Chang Chen;  Lei Wang;  Jian-Ying Wang;  Yu-Yu Niu;  Yi-Qiang Cui;  Zhou JK(周建奎);  #Hong Wang;  Xue-Jiang Guo;  Hu B(胡边);  Zhou Q(周琪);  Sha JH(沙家豪);  Ji WZ(季维智);  Huang XX(黄行许)
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Wt1 Functions in Ovarian Follicle Development by Regulating Granulosa Cell Differentiation 期刊论文
Human Molecular Genetics, 2014, 卷号: 23, 期号: 2, 页码: 333-341
Authors:  Gao F(高飞);  Zhang J(张君);  Wang XN(王晓娜);  Yang JL(杨俊玲);  Chen DH(陈大华);  V.Huff;  Liu YX(刘以训)
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A Feed-Forward Mechanism Involving Drosophila Fragile X Mental Retardation Protein Triggers a Replication Stress-Induced DNA Damage Response 期刊论文
Human Molecular Genetics, 2014, 卷号: 23, 期号: 19, 页码: 5188-5196
Authors:  Zhang WX(章文信);  Cheng Y(程郢);  Yu-Jing Li;  Chen ZP(陈振平);  Jin P(金鹏);  Chen DH(陈大华)
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Genome-Wide Loss of 5-hmC Is a Novel Epigenetic Feature of Huntingtons Disease 期刊论文
Human Molecular Genetics, 2013, 卷号: 22, 期号: 18, 页码: 3641-3653
Authors:  Wang FL(王凤丽);  Ye-Ran Yang;  Lin XW(林羲雯);  Wang JQ(王久强);  Yong-Sheng Wu;  Xie WJ(谢文娟);  Dan-Dan Wang;  Zhu S(朱姝);  You-Qi Liao;  Sun QM(孙钦秒);  Yang YG(杨运桂);  Luo HR(罗怀容);  Guo CX(郭彩霞);  Han CS(韩春生);  Tang TS(唐铁山)
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Genome-Wide Loss of 5-hmC Is a Novel Epigenetic Feature of Huntingtons Disease 期刊论文
Human Molecular Genetics, 2013, 卷号: 22, 期号: 18, 页码: 3641-3653
Authors:  Wang FL(王凤丽);  Ye-Ran Yang;  Lin XW(林羲雯);  Wang JQ(王久强);  Yong-Sheng Wu;  Xie WJ(谢文娟);  Dan-Dan Wang;  Zhu S(朱姝);  You-Qi Liao;  Sun QM(孙钦秒);  Yang YG(杨运桂);  Luo HR(罗怀容);  Guo CX(郭彩霞);  Han CS(韩春生);  Tang TS(唐铁山)
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Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28 期刊论文
Human Molecular Genetics, 2011, 卷号: 20, 期号: 16, 页码: 3213-3226
Authors:  Han Y;  Mu Y;  Li X;  Xu P;  Tong J;  Liu Z;  Ma T;  Zeng G;  Yang S;  Du J;  Meng A
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Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28 期刊论文
Human Molecular Genetics, 2011, 卷号: 20, 期号: 16, 页码: 3213-3226
Authors:  Han YC;  Mu Y;  Li XQ;  Xu PF;  Tong JY;  Liu ZT;  Ma TT;  Zeng GD;  Yang SY;  Du JL;  Meng AM
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Small regulatory RNAs in neurodevelopmental disorders 期刊论文
Human Molecular Genetics, 2009, 卷号: 18, 期号: R18-R26
Authors:  Chang S;  Wen SM;  Chen DH;  Jin P
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The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits 期刊论文
Human Molecular Genetics, 2008, 卷号: 17, 期号: 13, 页码: 2047-2057
Authors:  Allan AM;  Liang XM;  Luo YP;  Pak CH;  Li XK;  Szulwach KE;  Chen DH;  Jin P;  Zhao XY
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