Fucheng Li - Department of Prenatal Diagnostic Center Guangzhou Women and Children's Medical Center, Guangzhou Medical University

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论文共 40 篇作者统计合作学者相似作者

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Prenatal Diagnosis and Outcomes in Fetuses with Duplex Kidney

Chunling Ma,Ruibin Huang,Fang Fu,Hang Zhou,You Wang,Shujuan Yan,Fei Guo, Huanyi Chen,Lushan Li,Xiangyi Jing,Fucheng Li,Jin Han,

INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICSno. 1 (2024): 353-359

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Prenatal Diagnosis in Fetal Right Aortic Arch Using Chromosomal Microarray Analysis and Whole Exome Sequencing: a Chinese Single-Center Retrospective Study

Lu Zhang,Ruibin Huang,Hang Zhou,Xiaomei Lin,Fei Guo,Xiangyi Jing,Yongling Zhang,Fucheng Li,Fatao Li,Qiuxia Yu,Dan Wang,Guilan Chen,

MOLECULAR CYTOGENETICSno. 1 (2024)

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Prenatal Diagnosis of Polycystic Renal Diseases: Diagnostic Yield, Novel Disease-Causing Variants, and Genotype-Phenotype Correlations

Ruibin Huang,Fang Fu,Fei Guo,Hang Zhou,Qiuxia Yu,Shujuan Yan,Liyuan Liu, Jianqin Lu,Chunling Ma,You Wang, Huanyi Chen,Dan Wang,

AMERICAN JOURNAL OF OBSTETRICS & GYNECOLOGY MFMno. 1 (2024)

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Early Prenatal Diagnosis of Spondylocostal Dysostosis Caused by a Novel Variant in MESP2

Yanhong Zhou,Guilan Chen,Fucheng Li,Li Huang,Jin Han

CONGENITAL ANOMALIESno. 2 (2024): 61-62

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Association of Prenatal Cleft Lip and Palate Ultrasound Abnormalities with Copy Number Variants at a Single Chinese Tertiary Center

Shujuan Yan,Qiuxia Yu,Hang Zhou,Ruibin Huang,You Wang,Chunling Ma,Fei Guo,Fang Fu,Ru Li,Fucheng Li, Xiangyi Jin,Li Zhen,

The Italian Journal of Pediatrics/Italian journal of pediatricsno. 1 (2024)

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Prenatal Diagnosis of 17q12 Copy Number Variants in Fetuses Via Chromosomal Microarray Analysis - a Retrospective Cohort Study and Literature Review

Ruibin Huang,Chunling Ma, Huanyi Chen,Fang Fu,Jin Han,Liyuan Liu,Lushan Li,Shujuan Yan, Jianqin Lu,Hang Zhou,You Wang,Fei Guo,

Heliyonpp.e36558, (2024)

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Ndufa4 Regulates the Proliferation and Apoptosis of Neurons Via Mir-145A-5p/homer1/ccnd2

Fu Fang, Chen,Du Kun,Li Lu-shan,Li Ru,Lei Ting-ying,Deng Qiong,Wang Dan,Yu Qiu-xia,Yang Xin,Han Jin,Pan Min,

MOLECULAR NEUROBIOLOGYno. 6 (2023): 2986-3003

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Variant Spectrum of F8 and F9 in Hemophilia Patients from Southern China and 26 Novel Variants

Fucheng Li,Liya He,Guilan Chen,Yan Lu,Ru Li,Yongling Zhang,Xiangyi Jing,Rujuan Ling,Dongzhi Li,Can Liao

FRONTIERS IN GENETICS (2023)

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Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing

Yingdi Liu,Dongzhi Li,Dongyi Yu,Qiaowei Liang,Guilan Chen,Fucheng Li, Lu Gao,Zhuo Li,Tiantian Xie, Le Wu,Aiping Mao,Lingqian Wu,

THROMBOSIS AND HAEMOSTASISno. 12 (2023): 1151-1164

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Case Report: Early Diagnosis of Lethal Multiple Pterygium Syndrome with Micrognathia: Two Novel Mutations in the CHRND Gene

Caiyuan Chen,Jin Han,Jiaxin Xue,Ru Li,Guilan Chen,Xin Yang,Jiajie Tang,Fucheng Li,Dongzhi Li

FRONTIERS IN GENETICS（2023）

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