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    First Thai Case of Lethal Desbuquois Dysplasia Type I Caused by Novel Compound Heterozygous CANT1 Mutations: Expanding the Molecular Spectrum

    Published in Case Reports in Genetics (2026)
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    The Ketogenic Diet in the Neonatal Intensive Care Setting: The Case of a Preterm Newborn With Mitochondrial DNA Depletion Syndrome Type 13 (MTDPS13)

    Published in Case Reports in Genetics (2026)
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    Concomitant Chromosomal and Molecular Aberrations in Trisomy 8 Mosaicism and Associated Compound Phenotypes: Report of Three Cases and Review of Literature

    Published in Case Reports in Genetics (2026)
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    Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum

    Published in Case Reports in Genetics (2026)
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    Phenotypic Spectrum of Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) in Denmark: A Case Series Characterizing the First Danish Families With the APC Promotor...

    Published in Case Reports in Genetics (2026)
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    Identification of a Novel DNAAF3 Variant in a 54-Year-Old Patient With Newly Diagnosed Primary Ciliary Dyskinesia (PCD)

    Published in Case Reports in Genetics (2026)
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    Correction to “Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India”

    Published in Case Reports in Genetics (2025)
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    Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature

    Published in Case Reports in Genetics (2025)
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    MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2

    Published in Case Reports in Genetics (2025)
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    A Complex Chromosome Rearrangement Disrupting SYT1 Supports Haploinsufficiency as a Cause of Baker–Gordon Syndrome

    Published in Case Reports in Genetics (2025)
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    Diaphragmatic Hernia in a Newborn With COL1A1-Associated Classical Ehlers–Danlos Syndrome

    Published in Case Reports in Genetics (2025)
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    Long-Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia

    Published in Case Reports in Genetics (2025)
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    Kufor–Rakeb Syndrome in a Guatemalan Patient With an ATP13A2 Gene Pathogenic Variant: A Case Report

    Published in Case Reports in Genetics (2025)
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    Genome survey and chromosome number determination of Polygala fallax (Polygalaceae), an endemic medicinal plant from southern China

    Published in Comparative Cytogenetics (2026)
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    Additional data of cryptic species of the blind mole rat (Nannospalax, Rodentia) (2n = 52, NF = 84) from the Eastern Anatolia Region of Türkiye

    Published in Comparative Cytogenetics (2026)
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    Cytogenetic analysis of some species of Cyphomyrmex Mayr, 1862 and Apterostigma Mayr, 1865 (Formicidae, Myrmicinae) from the Guiana Shield

    Published in Comparative Cytogenetics (2026)
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    Chromosomes of Aganaspis daci (Weld, 1951) and a review of known karyotypes of the family Figitidae (Hymenoptera)

    Published in Comparative Cytogenetics (2026)
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    The forbidden doubling: exploring rare spermatocyte polyploidy in mammals

    Published in Comparative Cytogenetics (2026)
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    On the anniversary of Professor, Dr. Sci. Valentina G. Kuznetsova, Editor-in-Chief of the journal “Comparative Cytogenetics”

    Published in Comparative Cytogenetics (2026)
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    Seven new karyotypes for subfamily Cercosaurinae (Squamata, Gymnophthalmidae) with a synthesis of chromosomal data

    Published in Comparative Cytogenetics (2026)
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