Frontiers in Genetics | Cytogenomics

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

2,920 views

Opinion

Published on 28 Feb 2024

Sometimes karyotype resolves the case!

in Cytogenomics

Laura Rodríguez
Elena Barros
Jesica Skaarup Murray

Frontiers in Genetics

doi 10.3389/fgene.2024.1371166

2,825 views
1 citation

Case Report

Published on 23 Feb 2024

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature

in Cytogenomics

Fatima Ouboukss
Zhour El Amrani
Hicham Bouchahta
Ilham Ratbi
Aziza Sbiti
Thomas Liehr
Abdelaziz Sefiani
Abdelhafid Natiq

Frontiers in Genetics

doi 10.3389/fgene.2024.1331676

3,315 views

Case Report

Published on 06 Feb 2024

Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review

in Cytogenomics

Chiara Minotti
Ludovico Graziani
Ester Sallicandro
Maria Cristina Digilio
Roberto Falasca
Viola Alesi
Giuseppe Novelli
Maria Lisa Dentici
Sara Loddo
Antonio Novelli

Frontiers in Genetics

doi 10.3389/fgene.2023.1315291

3,055 views
1 citation

Brief Research Report

Published on 08 Jan 2024

Small supernumerary marker chromosomes in prenatal diagnosis—molecular characterization and clinical outcomes

in Cytogenomics

Ivana Joksic
Mina Toljic
Iva Milacic
Andjela Stankovic
Natasa Karadzov Orlic
Zeljko Mikovic

Frontiers in Genetics

doi 10.3389/fgene.2023.1326985

2,888 views
5 citations

Original Research

Published on 15 Dec 2023

Small supernumerary marker chromosomes derived from human chromosome 11

in Cytogenomics

Thomas Liehr
Monika Ziegler
Luisa Person
Stefanie Kankel
Niklas Padutsch
Anja Weise
Jörg Paul Weimer
Heather Williams
Susana Ferreira
Joana B. Melo

Frontiers in Genetics

doi 10.3389/fgene.2023.1293652

3,891 views
3 citations

Original Research

Published on 14 Dec 2023

Clinical application of single nucleotide polymorphism microarray analysis in pregnancy loss in Northwest China

in Cytogenomics

ShuYuan Xue
LiXia Wang
Jie Wei
YuTong Liu
GuiFeng Ding
PengGao Dai

Frontiers in Genetics

doi 10.3389/fgene.2023.1319624

3,095 views
4 citations

Hypothesis and Theory

Published on 24 Nov 2023

Hypothesis: The opposing pulling forces exerted by spindle microtubules can cause sliding of chromatin layers and facilitate sister chromatid resolution

in Cytogenomics

Joan-Ramon Daban

Frontiers in Genetics

doi 10.3389/fgene.2023.1321260

2,277 views
1 citation

Original Research

Published on 24 Nov 2023

Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing

in Cytogenomics

You Wang
Ru Li
Fang Fu
Ruibin Huang
Dongzhi Li
Can Liao

Frontiers in Genetics

doi 10.3389/fgene.2023.1260995

6,024 views
4 citations

Opinion

Published on 10 Oct 2023

Be careful with small supernumerary marker chromosomes!

in Cytogenomics

Laura Rodríguez

Frontiers in Genetics

doi 10.3389/fgene.2023.1269679

4,536 views
2 citations

Original Research

Published on 13 Mar 2023

Effectiveness of non-invasive chromosomal screening for normal karyotype and chromosomal rearrangements

in Cytogenomics

Bo-lan Sun
Yong Wang
Sixi-Wen
Liang Zhou
Chun-hui Zhang
Ze-Xuan Wu
Jie Qiao
Qing-yuan Sun
Ya-xin Yao
Jing Wang

Frontiers in Genetics

doi 10.3389/fgene.2023.1036467

5,339 views
7 citations

35 articles

articles

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

Sometimes karyotype resolves the case!

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature

Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review

Small supernumerary marker chromosomes in prenatal diagnosis—molecular characterization and clinical outcomes

Small supernumerary marker chromosomes derived from human chromosome 11

Clinical application of single nucleotide polymorphism microarray analysis in pregnancy loss in Northwest China

Hypothesis: The opposing pulling forces exerted by spindle microtubules can cause sliding of chromatin layers and facilitate sister chromatid resolution

Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing

Be careful with small supernumerary marker chromosomes!

Effectiveness of non-invasive chromosomal screening for normal karyotype and chromosomal rearrangements