Paper Review Records
全部论文审稿周期
25 篇有效样本 · 按发表日期由新到旧排列
审稿天数=录用日期-收稿日期;保留 PDF/DOI/网页源链接
201
天
Rare Biallelic CTU2 Variants in an Individual With CAKUT : Clinical Characterization and Minigene Splicing Analysis
作者
Qian Liu; Xueqin Cheng; Bixia Zheng; Chunli Wang; Wei Zhou; Aihua Zhang展开收起
作者单位
1. Department of Nephrology Children's Hospital of Nanjing Medical University Nanjing Jiangsu China; 2. Nanjing Key Laboratory of Pediatrics Children's Hospital of Nanjing Medical University Nanjing Jiangsu China展开收起
313
天
A Synonymous DLG4 Variant (c. 771G >A) Causes Exon 9 Skipping via Paternal Germline Mosaicism in DLG4 ‐Related Synaptopathy
作者
Jing Chen; Qinfei Zhao; Xinyue Zhang; Nan Wu; Xuxiang Xi; Yin Zeng; Sa Wu; Kun Yuan; Zezhang Liu; Xiangsheng Wu; Shaoying Zeng展开收起
作者单位
1. Department of Laboratory Medicine First Affiliated Hospital of Gannan Medical University Ganzhou Jiangxi China; 2. Nanchang University Nanchang China; 3. The First School of Clinical Medicine Gannan Medical University Ganzhou Jiangxi China; 4. Department of Obstetrics and Gynecology First Affiliated Hospital of Gannan Medical University Ganzhou Jiangxi China; 5. BGI Genomics Shenzhen Guangdong China; 6. Clin Lab BGI Genomics Wuhan Hubei China展开收起
111
天
Knowledge Mapping of Alport Syndrome: A Bibliometric Analysis From 2000 to 2025
作者
Xiujuan Cao; Wei Zhou; Yong Wang; Lvxian Wu; Jianhua Mao展开收起
作者单位
1. Department of Nephrology, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center Hangzhou Zhejiang China; 2. Department of Pediatrics Jinhua Municipal Central Hospital Jinhua China; 3. The Key Laboratory for Screening and Diagnosis of Maternal and Child Genetic Disease of Health Commission of Jiangxi Province Jiujiang Jiangxi China; 4. Department of Internal Medicine Yanbian University Hospital Yanji Jilin China展开收起
156
天
Identification of the MYH6 c. 804G >C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family
作者
Songlin Zhang; Xiaohua Tang; Leixiang Yang; Yang Wang; Yong Cui; Xiaopan Chen展开收起
作者单位
1. Laboratory Medicine Center, Department of Genetic and Genomic Medicine Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College Hangzhou Zhejiang China; 2. Key Laboratory of Birth Defects Wenzhou Central Hospital Wenzhou Zhejiang China; 3. Heart Center, Department of Cardiovascular Surgery Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College Hangzhou Zhejiang China展开收起
124
天
349
天
Body Region Dysmorphology Is Predictive of Genetic Diagnoses in Infants With Congenital Heart Disease
作者
Benjamin M. Helm; Leah Wetherill; Benjamin J. Landis; Stephanie M. Ware展开收起
作者单位
1. Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA; 2. Department of Pediatrics Indiana University School of Medicine Indianapolis Indiana USA展开收起
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