Search Results - "— — — — — — Genetics"

  1. A Complex Chromosome Rearrangement Disrupting SYT1 Supports Haploinsufficiency as a Cause of Baker–Gordon Syndrome

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  2. Diaphragmatic Hernia in a Newborn With COL1A1-Associated Classical Ehlers–Danlos Syndrome

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  3. Long-Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  4. 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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  5. Identification of a Mosaic BMPR1A Pathogenic Variant in Juvenile Polyposis Syndrome: A Case Study and Its Impact on Cancer Screening

    Published in Case Reports in Genetics (2025)
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  6. Identification of a Rare Variant in the SRD5A2 Gene in Siblings With 46,XY Disorders of Sexual Development

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  7. Novel SIAH1 Frameshift Variant in a Chilean Patient With Buratti–Harel Syndrome

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  8. RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  9. Bone Marrow Failure Associated With Short Telomeres and Digenic Variants of Uncertain Significance in Telomere Biology Genes

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  10. A Novel Variant in the BICRA Gene, Expanding the Phenotype: A Case Report

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  11. Emanuel Syndrome: A Case Report With Isolated Nuchal Translucency Thickening

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  12. Mitochondrial Dysfunction in Sickle Cell Trait Carriers With Exertional Collapse

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  13. An Extremely Preterm Infant With PIK3CA-Related Overgrowth Spectrum (PROS): Alpelisib Treatment and Outcome

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  14. A Novel Case of NOTCH1 Variant and Nonimmune Hydrops Fetalis: A Case Report

    Published in Case Reports in Genetics (2025)
    Subjects: “…— — — — — — Genetics…”
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  15. Genome survey and chromosome number determination of Polygala fallax (Polygalaceae), an endemic medicinal plant from southern China

    Published in Comparative Cytogenetics (2026)
    Subjects: “…— — — — — — Genetics…”
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  16. 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)
    Subjects: “…— — — — — — Genetics…”
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  17. Cytogenetic analysis of some species of Cyphomyrmex Mayr, 1862 and Apterostigma Mayr, 1865 (Formicidae, Myrmicinae) from the Guiana Shield

    Published in Comparative Cytogenetics (2026)
    Subjects: “…— — — — — — Genetics…”
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  18. Chromosomes of Aganaspis daci (Weld, 1951) and a review of known karyotypes of the family Figitidae (Hymenoptera)

    Published in Comparative Cytogenetics (2026)
    Subjects: “…— — — — — — Genetics…”
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  19. The forbidden doubling: exploring rare spermatocyte polyploidy in mammals

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

    Published in Comparative Cytogenetics (2026)
    Subjects: “…— — — — — — Genetics…”
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