G Banding | List of Frontiers open access articles

Case Report

Published on 17 Dec 2025

Case Report: Prenatal diagnosis of a rare complex fetal karyotype 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat resulting from 3:1 meiotic segregation of a maternal balanced translocation

in Gynecology

G. S. Deng
D. H. Zhang
Y. Q. Lai
J. J. Song
J. J. Pan
X. F. Liang
Y. H. Lu
S. S. Ning
W. C. Li
X. Li

Frontiers in Reproductive Health

doi 10.3389/frph.2025.1737392

579 views

Case Report

Published on 10 Dec 2024

Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7

in Pediatric Endocrinology

Takashi Shoji
Ichiro Yamauchi
Hidenori Kawasaki
Kogoro Iwanaga
Takuro Hakata
Daisuke Tanaka
Junji Fujikura
Toshihiko Masui
Hisato Suzuki
Mamiko Yamada

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1431547

3,104 views

Case Report

Published on 18 Jul 2024

Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review

in Cytogenomics

Rong Hua Wang
Ke Wu
Xiao Ling Hu

Frontiers in Genetics

doi 10.3389/fgene.2024.1436469

2,320 views

Original Research

Published on 24 Feb 2022

Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review

in Genetics of Common and Rare Diseases

Yi Liang
Yingjun Xie
Shu Kong
Qianying Pan
Wenjun Qiu
Ding Wang
Mengting Li
Sisi Lin
Zihang Liu
Xiaofang Sun

Frontiers in Genetics

doi 10.3389/fgene.2022.792539

4,505 views
12 citations

Methods

Published on 01 Jul 2025

Chromosomal quality control in hPSCs: A practical guide to SNP array analysis with GenomeStudio

in Stem Cell Research

Josephine Haake
Laura Steenpass

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2025.1599923

2,883 views
3 citations

Original Research

Published on 04 Mar 2021

SINO Syndrome Causative KIDINS220/ARMS Gene Regulates Adipocyte Differentiation

in Epigenomics and Epigenetics

Kaihui Zhang
Wenxing Sun
Yi Liu
Yuqiang Lv
Daisen Hou
Yan Lin
Wei Xu
Jianyuan Zhao
Zhongtao Gai
Shimin Zhao

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2021.619475

10,470 views
15 citations

Case Report

Published on 11 Nov 2022

Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature

in Genetics of Common and Rare Diseases

Chariyawan Charalsawadi
Somchit Jaruratanasirikul
Areerat Hnoonual
Aussanai Chantarapong
Pornsiri Sangmanee
Sasipong Trongnit
Natini Jinawath
Pornprot Limprasert

Frontiers in Genetics

doi 10.3389/fgene.2022.802362

8,786 views
5 citations

Original Research

Published on 21 Dec 2021

Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees

in Human and Medical Genomics

Huamei Hu
Rong Zhang
Yongyi Ma
Yanmei Luo
Yan Pan
Juchun Xu
Lupin Jiang
Dan Wang

Frontiers in Genetics

doi 10.3389/fgene.2021.731815

5,697 views
3 citations

Original Research

Published on 08 May 2025

Clinical features and genetic analysis of a family with t(5;9) (p15;p24) balanced translocation leading to Cri-du-chat syndrome in offspring

in Genetics of Common and Rare Diseases

Jing Zhao
Ping Chen
Yijia Ren
Shurong Li
Weiyi Zhang
Yan Li
Fengyu Wang

Frontiers in Genetics

doi 10.3389/fgene.2025.1550937

3,475 views
1 citation

Case Report

Published on 14 Nov 2025

Familial Xq27.1q28 duplication arising from a maternal interarm forward insertion of the X chromosome: a case report

in Genetics of Common and Rare Diseases

Xiang Li
Yuan-Mei Peng
Bo-Wen Luo
Yu-Di Luo
Yun-Rong Qin
Keng Feng
De-Rong Li
Zeng-Yu Yang
Ling-Ling Zhu
Jin-Jie Pan

Frontiers in Genetics

doi 10.3389/fgene.2025.1514856

1,584 views

Brief Research Report

Published on 02 Apr 2025

Optical genome mapping with whole genome sequencing identifies complex chromosomal structural variations in acute leukemia

in Genomic Assay Technology

Meng-Ju Melody Tsai
Hsiao-Jung Kao
Hsiao-Huei Chen
Chih-Hsiang Yu
Yin-Hsiu Chien
Wuh-Liang Hwu
Pui-Yan Kwok
Ni-Chung Lee
Yung-Li Yang

Frontiers in Genetics

doi 10.3389/fgene.2025.1496847

4,603 views
3 citations

Case Report

Published on 19 Feb 2020

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China

in Genetics of Common and Rare Diseases

Jianlian Deng
Haoqing Zhang
Caiyun Li
Hui Huang
Saijun Liu
Huanming Yang
Kaili Xie
Qiong Wang
Dongzhu Lei
Jing Wu

Frontiers in Genetics

doi 10.3389/fgene.2019.01350

35,292 views
6 citations

Case Report

Published on 14 Nov 2025

Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the SPTB gene that causes hereditary spherocytosis with hemolytic anemia

in Genetics of Common and Rare Diseases

Ke Cao
Xiaojuan Luo
Lianlian Liu
Xiaoning Mao
Ruping Liu
Yunsheng Chen
Santasree Banerjee

Frontiers in Genetics

doi 10.3389/fgene.2025.1626155

1,385 views

Original Research

Published on 28 Jun 2022

Molecular Profiling of Kenyan Acute Myeloid Leukemia Patients

in Human and Medical Genomics

Mercy Gatua
Mohsen Navari
Matilda Ong’ondi
Noel Onyango
Serah Kaggia
Emily Rogena
Giuseppe Visani
Nicholas A. Abinya
Pier Paolo Piccaluga

Frontiers in Genetics

doi 10.3389/fgene.2022.843705

4,445 views
4 citations

Case Report

Accepted on 27 Feb 2026

Prenatal Genetic Analysis of a Rare Fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) Karyotype

in Genetics of Common and Rare Diseases

Guosheng Deng
Xiafei Liang
Yuqing Lai
Jujie Song
Jinjie Pan
Yinghong Lu
Lili Li
YN Liang

Frontiers in Genetics

Original Research

Published on 09 May 2024

Prenatal diagnosis and pregnancy outcomes in fetuses with ventriculomegaly

in Obstetrics and Gynecology

Fagui Yue
Xiao Yang
Ning Liu
Ruizhi Liu
Hongguo Zhang

Frontiers in Medicine

doi 10.3389/fmed.2024.1349171

3,307 views
4 citations

Articles

Case Report: Prenatal diagnosis of a rare complex fetal karyotype 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat resulting from 3:1 meiotic segregation of a maternal balanced translocation

Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7

Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review

Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review

Chromosomal quality control in hPSCs: A practical guide to SNP array analysis with GenomeStudio

SINO Syndrome Causative KIDINS220/ARMS Gene Regulates Adipocyte Differentiation

Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature

Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees

Clinical features and genetic analysis of a family with t(5;9) (p15;p24) balanced translocation leading to Cri-du-chat syndrome in offspring

Familial Xq27.1q28 duplication arising from a maternal interarm forward insertion of the X chromosome: a case report

Optical genome mapping with whole genome sequencing identifies complex chromosomal structural variations in acute leukemia

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China

Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the SPTB gene that causes hereditary spherocytosis with hemolytic anemia

Molecular Profiling of Kenyan Acute Myeloid Leukemia Patients

Prenatal Genetic Analysis of a Rare Fetus with 45, X/46, X, dic r (Y; Y)/46, X, r(Y) Karyotype

Prenatal diagnosis and pregnancy outcomes in fetuses with ventriculomegaly