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  1. 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)
    Subjects: “…Biological Sciences…”
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  2. Correction to “Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India”

    Published in Case Reports in Genetics (2025)
    Subjects: “…Biological Sciences…”
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  3. 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)
    Subjects: “…Biological Sciences…”
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  4. MCT8 Deficiency in Two Brothers With a Novel Deletion Mutation in SLC16A2

    Published in Case Reports in Genetics (2025)
    Subjects: “…Biological Sciences…”
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  5. A Complex Chromosome Rearrangement Disrupting SYT1 Supports Haploinsufficiency as a Cause of Baker–Gordon Syndrome

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

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

    Published in Case Reports in Genetics (2025)
    Subjects: “…Biological Sciences…”
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  8. Kufor–Rakeb Syndrome in a Guatemalan Patient With an ATP13A2 Gene Pathogenic Variant: A Case Report

    Published in Case Reports in Genetics (2025)
    Subjects: “…Biological Sciences…”
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  9. 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)
    Subjects: “…Biological Sciences…”
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  10. 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: “…Biological Sciences…”
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  11. Novel SIAH1 Frameshift Variant in a Chilean Patient With Buratti–Harel Syndrome

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

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

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

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

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

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

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

    Published in Comparative Cytogenetics (2026)
    Subjects: “…Biological Sciences…”
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  19. 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: “…Biological Sciences…”
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  20. 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: “…Biological Sciences…”
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