Publications by authors named "Congmian Ren"

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Epigenetic phenotype of plasma cell-free DNA in the prediction of early-onset preeclampsia.
Wei He, Yi Zhang, Kai Wu, Yunan Wang, Xin Zhao, Congmian Ren

J Obstet Gynaecol· December 2023

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Shortened fetal long bones: A notable intrauterine phenotypic feature in SHOX-associated skeletal dysplasia.
Rong Hu, Weiwei Huang, Congmian Ren, Ling Liu, Yaping Hou

Prenat Diagn· September 2023

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[Prenatal diagnosis and genetic analysis of three fetuses with paternal chromosomal simplex 3q microduplication syndrome].
Laiping Zheng, Congmian Ren, Fangmei Xu, Li Guo, Ting Wang

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2022

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Phenotypic findings and pregnancy outcomes of fetal rare autosomal aneuploidies detected using chromosomal microarray analysis.
Rong Hu, Weiwei Huang, Weining Zhou, Xiaohui Luo, Congmian Ren

Hum Genomics· December 2022

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Clinical and molecular cytogenetic findings and pregnancy outcomes of fetuses with isochromosome Y.
Yiqun He, Li Guo, Laiping Zheng, Congmian Ren, Ting Wang

Mol Cytogenet· August 2022

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Prenatal diagnosis of mosaic trisomy 2 and literature review.
Ting Wang, Jufei Lian, Congmian Ren, Huamei Huang, Yanlin Huang

Mol Cytogenet· August 2020

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Prenatal diagnosis of Pallister-Killian syndrome using cord blood samples.
Ting Wang, Congmian Ren, Dan Chen, Jian Lu, Li Guo

Mol Cytogenet· August 2019

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[Combined chromosomal microarray analysis and fluorescence in situ hybridization for prenatal diagnosis of two cases with Pallister-Killian syndrome].
Ting Wang, Congmian Ren, Li Guo, Jian Lu, Hanbiao Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2019

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Balanced translocation t(3;18)(p13;q22.3) and points mutation in the ZNF407 gene detected in patients with both moderate non-syndromic intellectual disability and autism.
Cong-mian Ren, Yan Liang, Fengxiang Wei, Ya-nan Zhang, Shou-qiang Zhong

Biochim Biophys Acta· March 2013

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