Prenatal diagnosis of Coffin‐Siris syndrome: What are the fetal features?
Yu, Qiu‐Xia, Jing, Xiang‐Yi, Lin, Xiao‐Mei, Zhen, Li, Li, Dong‐Zhi
Published in Prenatal diagnosis (01.11.2022)
Published in Prenatal diagnosis (01.11.2022)
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Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease
Fu, Fang, Li, Ru, Lei, Ting-ying, Wang, Dan, Yang, Xin, Han, Jin, Pan, Min, Zhen, Li, Li, Jian, Li, Fa-tao, Jing, Xiang-yi, Li, Dong-zhi, Liao, Can
Published in Human genetics (01.02.2021)
Published in Human genetics (01.02.2021)
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Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series
Jing, Xiang-Yi, Huang, Lv-Yin, Zhen, Li, Han, Jin, Li, Dong-Zhi
Published in Journal of obstetrics and gynaecology (03.04.2019)
Published in Journal of obstetrics and gynaecology (03.04.2019)
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The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study
Fu, Fang, Li, Ru, Yu, Qiu-Xia, Dang, Xiao, Yan, Shu-Juan, Zhou, Hang, Cheng, Ken, Huang, Rui-Bin, Wang, You, Zhang, Yong-Ling, Jing, Xiang-Yi, Zhang, Li-Na, Li, Dong-Zhi, Liao, Can
Published in Genes (01.12.2022)
Published in Genes (01.12.2022)
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Improved outcomes in patients with prenatally detected 22q11.2 deletion syndrome
Jing, Xiang-Yi, Li, Dong-Zhi
Published in American journal of obstetrics and gynecology (01.04.2024)
Published in American journal of obstetrics and gynecology (01.04.2024)
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Prenatal diagnosis of Smith–Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects
Lei, Ting-Ying, Li, Ru, Fu, Fang, Wan, Jun-Hui, Zhang, Yong-Ling, Jing, Xiang-Yi, Liao, Can
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
Published in Taiwanese journal of obstetrics & gynecology (01.12.2016)
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Sotos syndrome: A study of antenatal presentation
Zhang, Yong-Ling, Jing, Xiang-Yi, Chen, Gui-Lan, Zhen, Li, Li, Dong-Zhi
Published in European journal of obstetrics & gynecology and reproductive biology (01.12.2022)
Published in European journal of obstetrics & gynecology and reproductive biology (01.12.2022)
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Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2
Fu, Fang, Chen, Chen, Du, Kun, Li, Lu-shan, Li, Ru, Lei, Ting-ying, Deng, Qiong, Wang, Dan, Yu, Qiu-xia, Yang, Xin, Han, Jin, Pan, Min, Zhen, Li, Zhang, Li-na, Li, Jian, Li, Fa-tao, Zhang, Yong-ling, Jing, Xiang-yi, Li, Fu-cheng, Li, Dong-zhi, Liao, Can
Published in Molecular neurobiology (01.06.2023)
Published in Molecular neurobiology (01.06.2023)
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Prenatal Silver-Russell Syndrome in a Chinese Family Identified by Non-Invasive Prenatal Testing
Zhang, Yong-Ling, Jing, Xiang-Yi, Wan, Jun-Hui, Pan, Min, Li, Dong-Zhi
Published in Molecular syndromology (01.07.2022)
Published in Molecular syndromology (01.07.2022)
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Prenatal diagnosis of trisomy 18 rescue resulting in mosaic of two different diploid cell lines in a hydropic fetus
Deng, Qiong, Li, Ru, Fu, Fang, Li, Fa-tao, Jing, Xiang-yi, Liao, Can
Published in European journal of obstetrics & gynecology and reproductive biology (01.05.2018)
Published in European journal of obstetrics & gynecology and reproductive biology (01.05.2018)
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NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathway
Fu, Fang, Li, Yan, Li, Ru, Lei, Ting-Ying, Wang, Dan, Yang, Xin, Han, Jin, Pan, Min, Zhen, Li, Ou, Yan-Mei, Li, Jian, Li, Fao-Tao, Jing, Xiang-Yi, Li, Dong-Zhi, Liao, Can
Published in American journal of translational research (01.01.2018)
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Published in American journal of translational research (01.01.2018)
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Prenatal diagnosis of Miller-Dieker syndrome/PAFAH1B1-related lissencephaly: Ultrasonography and genetically investigative results
Zhang, Yong-Ling, Jing, Xiang-Yi, Zhen, Li, Pan, Min, Han, Jin, Li, Dong-Zhi
Published in European journal of obstetrics & gynecology and reproductive biology (01.07.2022)
Published in European journal of obstetrics & gynecology and reproductive biology (01.07.2022)
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