Original Research
Accepted on 02 Jul 2025
Identification of key genes associated with infertile endometriosis based on bioinformatic analysis
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1615268
- Frontiers in Genetics
- Cytogenomics
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31 articles
Original Research
Published on 25 Jun 2025
Application of chromosome microarray analysis and karyotyping in fetal cardiac abnormalities
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1611388
- 544 views
Original Research
Published on 23 Jun 2025
Directional genomic hybridization (dGH™) identifies small inverted duplications in situ
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1604822
- 597 views
Original Research
Published on 23 Jun 2025
Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1539902
- 660 views
Systematic Review
Published on 11 Jun 2025
Exome sequencing and prenatal skeletal abnormalities: comprehensive review and meta-analysis and way forward
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1502538
- 965 views
Original Research
Published on 30 May 2025
Hapten-labeled DNA probes can be stored and used in fluorescence in situ hybridization for decades
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1569308
- 1,251 views
Case Report
Published on 22 May 2025
Case Report: Optical genome mapping enables identification of complex balanced chromosomal rearrangements
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1555485
- 1,194 views
Original Research
Accepted on 13 May 2025
Intrauterine ultrasound phenotyping, molecular characteristics and postnatal follow-up of fetuses with the 1q21.1 microdeletion/microduplication syndrome: a single-center, retrospective clinical study and review of the literature
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1568225
- 171 views
Case Report
Published on 06 May 2025
Case Report: A prenatal case with sex discordance between non-invasive prenatal testing and fetal genetic testings due to maternal rare chromosome karyotype
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1546579
- 1,226 views
Original Research
Published on 25 Mar 2025
Karyotype and genome size analyses for two spiders of the lycosidae family
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1544087
- 1,393 views
Case Report
Published on 05 Mar 2025
Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1544565
- 1,078 views
Original Research
Published on 13 Jan 2025
Improving prenatal diagnosis with combined karyotyping, CNV-seq and QF-PCR: a comprehensive analysis of chromosomal abnormalities in high-risk pregnancies
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1517270
- 1,986 views
Original Research
Published on 15 Oct 2024
Prenatal diagnosis and postnatal follow-up of 15 fetuses with 16p13.11 microduplication syndrome
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1486974
- 2,240 views
- 1 citation
Case Report
Published on 19 Sep 2024
Case report: A novel FBXW7 gene variant causes global developmental delay
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1436462
- 1,711 views
- 2 citations
Original Research
Published on 29 Aug 2024
Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1448341
- 2,190 views
- 1 citation
Case Report
Published on 18 Jul 2024
Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1436469
- 1,423 views