Jianlong Zhuang (Wanyu Fu)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Transcription Factor

Particulate Matter

Top Venues

Molecular genetics & genomic medicine

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Birth defects research

Journal of clinical pathology

This page only lists publications with an associated author ORCID identifier.

Publications

Xinying Chen, Yuying Jiang, Shuhong Zeng, Jianlong Zhuang, Na Lin
Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis. Birth defects research 116 (5) (2024)
Nan Huang, Hegan Zhang, Zhengping Huang, Xiaoxia Wu, Na Zhang, Yuying Jiang, Chunnuan Chen, Jianlong Zhuang
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal Death. Birth defects research 116 (8) (2024)
Jianlong Zhuang, Yuying Jiang, Yu'e Chen, Aiping Mao, Junwei Chen, Chunnuan Chen
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population. Molecular genetics & genomic medicine 12 (1) (2024)
Jianlong Zhuang, Na Zhang, Junyu Wang, Yuying Jiang, Hegan Zhang, Chunnuan Chen
Initial clinical and molecular investigation of 20q13.33 microdeletion with 17q25.3/14q32.31q32.33 microduplication in Chinese pediatric patients. Molecular genetics & genomic medicine 12 (4) (2024)
Jianlong Zhuang, Yuying Jiang, Yu'e Chen, Aiping Mao, Junwei Chen, Chunnuan Chen
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population. Molecular genetics & genomic medicine 12 (1) (2024)
Jianlong Zhuang, Shufen Liu, Junyu Wang, Yu'e Chen, Hegan Zhang, Yuying Jiang, Gaoxiong Wang, Chunnuan Chen
Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome. Molecular genetics & genomic medicine (2023)
Jianlong Zhuang, Qi Luo, Meihua Xie, Yu'e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review. Molecular genetics & genomic medicine (2022)
Jianlong Zhuang, Qi Luo, Meihua Xie, Yu'e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review. Molecular genetics & genomic medicine 11 (3) (2022)
Jianlong Zhuang, Qi Luo, Meihua Xie, Yu'e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review. Molecular genetics & genomic medicine 11 (3) (2022)
Jianlong Zhuang, Qi Luo, Meihua Xie, Yu'e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review. Molecular genetics & genomic medicine 11 (3) (2022)
Jianlong Zhuang, Qi Luo, Shuhong Zeng, Yu'e Chen, Shuxia Lin, Yuanbai Wang, Yuying Jiang
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign Variant. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 39 (1) (2022)
Jianlong Zhuang, Qi Luo, Shuhong Zeng, Yu'e Chen, Shuxia Lin, Yuanbai Wang, Yuying Jiang
A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign Variant. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 39 (1) (2022)
Jianlong Zhuang, Qi Luo, Meihua Xie, Yu'e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature review. Molecular genetics & genomic medicine 11 (3) (2022)
Jianlong Zhuang, Chunnuan Chen, Yuying Jiang, Qi Luo, Shuhong Zeng, Chunling Lv, Yuanbai Wang, Jianlong Zhuang
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China. BMC pregnancy and childbirth 21 (1) (2021)
Jianlong Zhuang, Yu Zheng, Yuanbai Wang, Qianmei Zhuang, Yuying Jiang, Qingyue Xie, Shuhong Zeng, Jianxing Zeng
Identification of a new β-thalassaemia variant Term CD+32(HBB: c.32A>C) in two Chinese families. Journal of clinical pathology 73 (9) (2020)
Jianlong Zhuang, Yuying Jiang, Yuanbai Wang, Yu Zheng, Qianmei Zhuang, Junyu Wang, Shuhong Zeng
Molecular analysis of α-thalassemia and β-thalassemia in Quanzhou region Southeast China. Journal of clinical pathology 73 (5) (2019)