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Songchang Chen

Showing results (21-30 of 65) with videos related to

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Prenatal Diagnosis|August 20, 2020
Should chromosomal microarray be offered to fetuses with ultrasonographic soft markers in second trimester: A prospective cohort study and meta-analysisShuyuan Li, Xu Han, Mujin Ye, et al.
Molecular Genetics & Genomic Medicine|July 23, 2021
Low-level germline mosaicism of a novel SMARCA2 missense variant: Expanding the phenotypic spectrum and mode of genetic transmissionNina Pan, Songchang Chen, Xiaoqiang Cai, et al.
Cellular and Molecular Life Sciences : CMLS|February 9, 2026
Role of RGS12 in placental mitochondrial dysfunction and adverse pregnancy outcomesXianling Cao, Xuanyou Zhou, Naixin Xu, et al.
Human Genomics|July 27, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disordersWenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
Journal of Medical Genetics|January 27, 2023
Parental mosaicism detection and preimplantation genetic testing in families with multiple transmissions of de novo mutationsNaixin Xu, Weihui Shi, Xianling Cao, et al.
Reproductive Biomedicine Online|May 21, 2021
Association of homocysteine with IVF/ICSI outcomes stratified by MTHFR C677T polymorphisms: a prospective cohort studyLuting Chen, Huixi Chen, Xiaojin Wang, et al.
Diagnostics (Basel, Switzerland)|June 12, 2026
A Fetal Fraction Optimized 106-Plex Digital PCR Assay for Non-Invasive Prenatal Testing of Fetal TrisomySongchang Chen, Xiaorui Luan, Xianling Cao, et al.
Reproductive Toxicology (Elmsford, N.Y.)|March 21, 2026
Phthalate mixtures and pregnancy loss: Linking MCNP exposure with placental dysfunction via epidemiologic and in vivo evidenceNaixin Xu, Peiran Hu, Weihui Shi, et al.
Mitochondrion|August 2, 2020
Associations of mitochondrial DNA copy number and deletion rate with early pregnancy lossMujin Ye, Weihui Shi, Yanhui Hao, et al.
Prenatal Diagnosis|January 17, 2019
Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysisShuyuan Li, Xu Han, Yanlin Wang, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|August 20, 2020
Should chromosomal microarray be offered to fetuses with ultrasonographic soft markers in second trimester: A prospective cohort study and meta-analysisShuyuan Li, Xu Han, Mujin Ye, et al.
Molecular Genetics & Genomic Medicine|July 23, 2021
Low-level germline mosaicism of a novel SMARCA2 missense variant: Expanding the phenotypic spectrum and mode of genetic transmissionNina Pan, Songchang Chen, Xiaoqiang Cai, et al.
Cellular and Molecular Life Sciences : CMLS|February 9, 2026
Role of RGS12 in placental mitochondrial dysfunction and adverse pregnancy outcomesXianling Cao, Xuanyou Zhou, Naixin Xu, et al.
Human Genomics|July 27, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disordersWenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
Journal of Medical Genetics|January 27, 2023
Parental mosaicism detection and preimplantation genetic testing in families with multiple transmissions of de novo mutationsNaixin Xu, Weihui Shi, Xianling Cao, et al.
Reproductive Biomedicine Online|May 21, 2021
Association of homocysteine with IVF/ICSI outcomes stratified by MTHFR C677T polymorphisms: a prospective cohort studyLuting Chen, Huixi Chen, Xiaojin Wang, et al.
Diagnostics (Basel, Switzerland)|June 12, 2026
A Fetal Fraction Optimized 106-Plex Digital PCR Assay for Non-Invasive Prenatal Testing of Fetal TrisomySongchang Chen, Xiaorui Luan, Xianling Cao, et al.
Reproductive Toxicology (Elmsford, N.Y.)|March 21, 2026
Phthalate mixtures and pregnancy loss: Linking MCNP exposure with placental dysfunction via epidemiologic and in vivo evidenceNaixin Xu, Peiran Hu, Weihui Shi, et al.
Mitochondrion|August 2, 2020
Associations of mitochondrial DNA copy number and deletion rate with early pregnancy lossMujin Ye, Weihui Shi, Yanhui Hao, et al.
Prenatal Diagnosis|January 17, 2019
Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysisShuyuan Li, Xu Han, Yanlin Wang, et al.
Pageof 7