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- [21] CLN8 Mutations Presenting with a Phenotypic Continuum of Neuronal Ceroid Lipofuscinosis-Literature Review and Case ReportGENES, 2021, 12 (07)Badura-Stronka, Magdalena论文数: 0 引用数: 0 h-index: 0机构: Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, Poland Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, PolandWinczewska-Wiktor, Anna论文数: 0 引用数: 0 h-index: 0机构: Poznan Univ Med Sci, Chair & Dept Dev Neurol, PL-60355 Poznan, Poland Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, PolandPietrzak, Anna论文数: 0 引用数: 0 h-index: 0机构: 10th Mil Res Hosp & Polyclin, Dept Neurol, PL-85681 Bydgoszcz, Poland Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, PolandHirschfeld, Adam Sebastian论文数: 0 引用数: 0 h-index: 0机构: Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, Poland Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, PolandZemojtel, Tomasz论文数: 0 引用数: 0 h-index: 0机构: Charite, BIH Genom Core Unit, Campus Mitte, D-13353 Berlin, Germany Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, PolandWolynska, Katarzyna论文数: 0 引用数: 0 h-index: 0机构: Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, Poland Poznan Univ Med Sci, Chair & Dept Med Genet, PL-60352 Poznan, Poland论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [22] A novel mutation in the ATP7B gene causing hepatolenticular degeneration in a Chinese family: A case reportMEDICINE, 2024, 103 (31) : e38849Zhou, Zhibo论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R China Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R ChinaZhang, Sainan论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R China Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R ChinaBi, Yunjiao论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Chinese Med Univ, Hangzhou, Peoples R China Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R ChinaDuan, Wenyuan论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Precis Med Testing Ctr,Key Lab Artificial Org, Hangzhou, Peoples R China Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R ChinaGao, Hainv论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R China Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Dept Infect Dis,Key Lab Artificial Organs & Comput, Hangzhou, Peoples R China
- [23] Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid LipofuscinosisFRONTIERS IN GENETICS, 2019, 10Ren, Xiao-Tun论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaWang, Xiao-Hui论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaDing, Chang-Hong论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaShen, Xiang论文数: 0 引用数: 0 h-index: 0机构: Running Gene Inc, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaZhang, Hao论文数: 0 引用数: 0 h-index: 0机构: Running Gene Inc, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaZhang, Wei-Hua论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaLi, Jiu-Wei论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaRen, Chang-Hong论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R ChinaFang, Fang论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing, Peoples R China
- [24] Novel variants identified in five Chinese families with Joubert Syndrome: a case reportBMC MEDICAL GENOMICS, 2023, 16 (01)Fang, Liwei论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R ChinaWang, Lulu论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R ChinaYang, Li论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R ChinaXu, Xiaoyan论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R ChinaPei, Shanai论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R ChinaWu, De论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China Anhui Med Univ, Affiliated Hosp 1, Pediat Neurorehabil Ctr, Pediat Dept, Hefei 230000, Peoples R China
- [25] A novel F8 variant in a Chinese hemophilia A family and involvement of X-chromosome inactivation: A case reportMEDICINE, 2023, 102 (18) : E33665Zhang, Honghong论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou 310014, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R ChinaLi, Yinjie论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R ChinaLv, Xiaojuan论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R ChinaMao, Yuchan论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Key Lab Reprod Genet, Minist Educ, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R ChinaSun, Yixi论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Key Lab Reprod Genet, Minist Educ, Hangzhou, Zhejiang, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Dept Reprod Genet, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R ChinaXu, Ting论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R China Hangzhou Childrens Hosp, Dept Pediat, Hangzhou, Zhejiang, Peoples R China
- [26] Case Report: Identification of a novel CASK missense variant in a Chinese family with MICPCHFRONTIERS IN GENETICS, 2022, 13Zhang, Runfeng论文数: 0 引用数: 0 h-index: 0机构: Hubei Normal Univ, Coll Life Sci, Huangshi, Hubei, Peoples R China Hubei Normal Univ, Coll Life Sci, Huangshi, Hubei, Peoples R ChinaJia, Peng论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Cardiol, Wuhan, Peoples R China Hubei Normal Univ, Coll Life Sci, Huangshi, Hubei, Peoples R ChinaYao, Yanyi论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hubei Prov, Ctr Med Genet, Wuhan, Peoples R China Hubei Normal Univ, Coll Life Sci, Huangshi, Hubei, Peoples R ChinaZhu, Feng论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Cardiol, Wuhan, Peoples R China Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Clin Ctr Human Gene Res, Wuhan, Peoples R China Hubei Normal Univ, Coll Life Sci, Huangshi, Hubei, Peoples R China
- [27] A novel mutation in a Chinese family with autosomal recessive Alport syndrome: a case reportINTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2019, 12 (09): : 3565 - 3569Sun, Huili论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaYu, Xuewen论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Pathol, 1 Fuhua Rd, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaLi, Shunmin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaXu, Hua论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Pathol, 1 Fuhua Rd, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaYang, Jun论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaYi, Tiegang论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaHan, Pengun论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R ChinaShao, Mumin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Pathol, 1 Fuhua Rd, Shenzhen 518033, Guangdong, Peoples R China Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Clin Med Coll 4, Dept Nephrol, Shenzhen 518033, Guangdong, Peoples R China
- [28] Case report: Novel compound heterozygous variants in the PANK2 gene in a Chinese patient diagnosed with ASD and ADHDFRONTIERS IN NEUROLOGY, 2023, 14Dong, Siqi论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Inst Neurol, Shanghai, Peoples R China Natl Ctr Neurol Disorders, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaTuo, Ya论文数: 0 引用数: 0 h-index: 0机构: Shanghai Univ Med & Hlth Sci, Dept Biochem & Physiol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaQi, Zihan论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Inst Neurol, Shanghai, Peoples R China Natl Ctr Neurol Disorders, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaZhang, Yuanfeng论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaLiu, Xiaoni论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Inst Neurol, Shanghai, Peoples R China Natl Ctr Neurol Disorders, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaHuang, Ping论文数: 0 引用数: 0 h-index: 0机构: Acad Forens Sci, Dept Forens Pathol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaChen, Xiangjun论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Inst Neurol, Shanghai, Peoples R China Natl Ctr Neurol Disorders, Shanghai, Peoples R China Fudan Univ, Human Phenome Inst, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China
- [29] Pathogenic variants of PROC gene caused type II activity deficiency in a Chinese family A case reportMEDICINE, 2021, 100 (12) : E25160Zhu, Hui论文数: 0 引用数: 0 h-index: 0机构: Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R China Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R ChinaLiu, Hongchao论文数: 0 引用数: 0 h-index: 0机构: Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R China Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R ChinaLiu, Jingyao论文数: 0 引用数: 0 h-index: 0机构: Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R China Jilin Univ, Hosp 1, Dept Neurol, Jilin Rd 3302, Changchun 130031, Peoples R China
- [30] Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese PatientsFRONTIERS IN GENETICS, 2021, 12Peng, Ying论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaLiang, Changbiao论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Hlth Care, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaXi, Hui论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaYang, Shuting论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaHu, Jiancheng论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaPang, Jialun论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaLiu, Jing论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaLuo, Yingchun论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaTang, Chengyuan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Hunan Prov Key Lab Kidney Dis & Blood Purificat, Dept Nephrol, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaXie, Wanqin论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R ChinaWang, Hua论文数: 0 引用数: 0 h-index: 0机构: Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Natl Hlth Commiss Key Lab Birth Defects Res & Pre, Changsha, Peoples R China