Xiaoyi Cong

Shenzhen, China

Last Updated: 09/26/2026

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Found 11 publications

How Are SNP-Array, Karyotyping, and FISH Applied in Prenatal Practice? A Focus on Diagnosis of Mosaicism Involving the Sex Chromosomes.

How Are SNP-Array, Karyotyping, and FISH Applied in Prenatal Practice? A Focus on Diagnosis of Mosaicism Involving the Sex Chromosomes.

Journal: Prenatal diagnosis

Published: December 13, 2025

Clinical analysis of prenatal diagnosis, ultrasound findings, and follow-up in 92 Turner mosaic fetuses: a retrospective analysis of 12-year experience.

Clinical analysis of prenatal diagnosis, ultrasound findings, and follow-up in 92 Turner mosaic fetuses: a retrospective analysis of 12-year experience.

Journal: BMC pregnancy and childbirth

Published: October 31, 2025

Evaluating the effectiveness of routine noninvasive prenatal screening for CNVs in 22q11.2 region in a cohort of 38,495 pregnancies.

Evaluating the effectiveness of routine noninvasive prenatal screening for CNVs in 22q11.2 region in a cohort of 38,495 pregnancies.

Journal: Scientific reports

Published: July 05, 2025

Prenatal Genetic Diagnosis of Williams-Beuren Syndrome with Atypical and Complex Phenotypes.

Prenatal Genetic Diagnosis of Williams-Beuren Syndrome with Atypical and Complex Phenotypes.

Journal: Clinical laboratory

Published: April 10, 2025

Genetic etiology and phenotypic characteristics of fetuses with 11q deletion syndrome (11q23.3-q25).

Genetic etiology and phenotypic characteristics of fetuses with 11q deletion syndrome (11q23.3-q25).

Journal: Experimental and therapeutic medicine

Published: April 07, 2025

A Whole MED12 Gene Deletion in a Female Fetus With Features Encountered in Hardikar Syndrome.

A Whole MED12 Gene Deletion in a Female Fetus With Features Encountered in Hardikar Syndrome.

Journal: Prenatal diagnosis

Published: September 17, 2024

Noninvasive prenatal screening and diagnosis of two fetuses with Williams syndrome in a cohort of 19,607 pregnancies.

Noninvasive prenatal screening and diagnosis of two fetuses with Williams syndrome in a cohort of 19,607 pregnancies.

Journal: Annals of medicine

Published: September 12, 2024

Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.

Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.

Journal: Archives of gynecology and obstetrics

Published: July 18, 2024

Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?

Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?

Journal: BMC pregnancy and childbirth

Published: December 07, 2023

Prenatal diagnosis, pregnancy determination and follow up of sex chromosome aneuploidy screened by non-invasive prenatal testing from 122 453 unselected singleton pregnancies: A retrospective analysis of 7-year experience.

Prenatal diagnosis, pregnancy determination and follow up of sex chromosome aneuploidy screened by non-invasive prenatal testing from 122 453 unselected singleton pregnancies: A retrospective analysis of 7-year experience.

Journal: Congenital anomalies

Published: May 16, 2023

Clinical characteristics and prenatal diagnosis of fetuses with sex chromosomal aneuploidies detected by non-invasive prenatal testing during early and midterm pregnancies

Clinical characteristics and prenatal diagnosis of fetuses with sex chromosomal aneuploidies detected by non-invasive prenatal testing during early and midterm pregnancies

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 09, 2021

Showing 1-11 of 11

Last Updated: 09/26/2026