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International Journal of Biological Macromolecules
|
September 13, 2025
Bioinspired PVA/CS/WPU@c-MWCNTs aerogel for concurrent highly efficient freshwater generation and hydrovoltaic power production
Pengzhen Jin, Chunyan Hu, Jian Zheng, et al.
Reproductive Biomedicine Online
|
April 28, 2024
Cytosine-guanine-guanine repeats of FMR1 gene negatively affect ovarian reserve and response in Chinese women
Xinyang Jin, Wenshan Zeng, Yanfei Xu, et al.
The Application of Clinical Genetics
|
June 23, 2026
Precise Reproductive Counseling Enabled by Long-Read Sequencing in a Case of a <i>F8</i> Intron 1 Inversion and Duplication
Yuying Yan, Pengzhen Jin, Lidan Xu, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis of a mosaic case with low proportion mutation of <i>TSC2</i> gene]
Xiaoxiao Jin, Pengzhen Jin, Kai Yan, et al.
Frontiers in Genetics
|
July 11, 2022
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)
Lihong Fan, Pengzhen Jin, Yeqing Qian, et al.
Molecular Cytogenetics
|
September 1, 2022
Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
Junjie Hu, Kai Yan, Pengzhen Jin, et al.
Frontiers in Immunology
|
September 3, 2025
Case Report: Prenatal diagnosis of gastrointestinal defects and immunodeficiency syndrome caused by compound heterozygous mutations in TTC7A gene
Shuning Han, Miaomiao Wang, Pengzhen Jin, et al.
BMC Pregnancy and Childbirth
|
September 9, 2024
Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies
Pengzhen Jin, Jiawei Hong, Yuqing Xu, et al.
Frontiers in Pediatrics
|
October 30, 2023
Case report: A compound heterozygous mutations in <i>ASNS</i> broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis
Linyan Zhu, Yixi Sun, Yuqing Xu, et al.
Molecular Syndromology
|
March 25, 2026
Whole Genome Sequence Identifies the Second Allele: An Intronic Variant in RYR1 Contributes to Early-Onset Fetal Akinesia Deformation Sequence
Miaomiao Wang, Jiawei Hong, Shuning Han, et al.
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Search research articles
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Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
International Journal of Biological Macromolecules
|
September 13, 2025
Bioinspired PVA/CS/WPU@c-MWCNTs aerogel for concurrent highly efficient freshwater generation and hydrovoltaic power production
Pengzhen Jin, Chunyan Hu, Jian Zheng, et al.
Reproductive Biomedicine Online
|
April 28, 2024
Cytosine-guanine-guanine repeats of FMR1 gene negatively affect ovarian reserve and response in Chinese women
Xinyang Jin, Wenshan Zeng, Yanfei Xu, et al.
The Application of Clinical Genetics
|
June 23, 2026
Precise Reproductive Counseling Enabled by Long-Read Sequencing in a Case of a <i>F8</i> Intron 1 Inversion and Duplication
Yuying Yan, Pengzhen Jin, Lidan Xu, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis of a mosaic case with low proportion mutation of <i>TSC2</i> gene]
Xiaoxiao Jin, Pengzhen Jin, Kai Yan, et al.
Frontiers in Genetics
|
July 11, 2022
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)
Lihong Fan, Pengzhen Jin, Yeqing Qian, et al.
Molecular Cytogenetics
|
September 1, 2022
Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
Junjie Hu, Kai Yan, Pengzhen Jin, et al.
Frontiers in Immunology
|
September 3, 2025
Case Report: Prenatal diagnosis of gastrointestinal defects and immunodeficiency syndrome caused by compound heterozygous mutations in TTC7A gene
Shuning Han, Miaomiao Wang, Pengzhen Jin, et al.
BMC Pregnancy and Childbirth
|
September 9, 2024
Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies
Pengzhen Jin, Jiawei Hong, Yuqing Xu, et al.
Frontiers in Pediatrics
|
October 30, 2023
Case report: A compound heterozygous mutations in <i>ASNS</i> broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis
Linyan Zhu, Yixi Sun, Yuqing Xu, et al.
Molecular Syndromology
|
March 25, 2026
Whole Genome Sequence Identifies the Second Allele: An Intronic Variant in RYR1 Contributes to Early-Onset Fetal Akinesia Deformation Sequence
Miaomiao Wang, Jiawei Hong, Shuning Han, et al.
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of 3