Ukc | List of Frontiers open access articles

Original Research

Published on 29 Jun 2023

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss

in Genetics of Common and Rare Diseases

Na Liao
Zhu Zhang
Xijing Liu
Jiamin Wang
Rui Hu
Like Xiao
Yunyuan Yang
Yi Lai
Hongmei Zhu
Lingping Li

Frontiers in Genetics

doi 10.3389/fgene.2023.1203891

4,919 views
6 citations

Original Research

Published on 10 Sep 2024

Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population

in Pediatric Urology

Yijing Chen
Lijun Zhou
Fang Chen
Zhongzhong Chen
Yichen Huang
Yiqing Lv
Min Wu
Xiaoling Lin
Hua Xie

Frontiers in Pediatrics

doi 10.3389/fped.2024.1409264

2,001 views
1 citation

Original Research

Published on 19 May 2021

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis

in Genomic Assay Technology

Sha Liu
Hongqian Liu
Jianlong Liu
Ting Bai
Xiaosha Jing
Tianyu Xia
Cechuan Deng
Yunyun Liu
Jing Cheng
Xiang Wei

Frontiers in Genetics

doi 10.3389/fgene.2021.666648

7,817 views
7 citations

Original Research

Published on 07 Mar 2024

High-resolution genomic profiling and locus-specific FISH in subcutaneous and visceral adipose tissue of obese patients

in Cytogenomics

Vivian-Pascal Brandt
Heidrun Holland
Matthias Blüher
Nora Klöting

Frontiers in Genetics

doi 10.3389/fgene.2023.1323052

3,364 views

Brief Research Report

Published on 14 Sep 2021

Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman With Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT

in Genomic Assay Technology

Line Dahl Jeppesen
Lotte Hatt
Ripudaman Singh
Palle Schelde
Lotte Andreasen
Sara Markholt
Dorte L. Lildballe
Ida Vogel

Frontiers in Genetics

doi 10.3389/fgene.2021.741752

10,505 views
10 citations

Case Report

Published on 31 Aug 2023

Case report: A case report and literature review of complete trisomy 9

in Genetics of Common and Rare Diseases

Chenxia Xu
Miaoyuan Li
Jianming Peng
Yanfang Zhang
Haijun Li
Guobing Zheng
Degang Wang

Frontiers in Genetics

doi 10.3389/fgene.2023.1241245

9,602 views
4 citations

Articles

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss

Novel evidence of CNV deletion in KCTD13 related to the severity of isolated hypospadias in Chinese population

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis

High-resolution genomic profiling and locus-specific FISH in subcutaneous and visceral adipose tissue of obese patients

Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman With Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT

Case report: A case report and literature review of complete trisomy 9