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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)Subjects: “…Biological Sciences…”
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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)Subjects: “…Biological Sciences…”
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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)Subjects: “…Biological Sciences…”
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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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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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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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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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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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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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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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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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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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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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Emanuel Syndrome: A Case Report With Isolated Nuchal Translucency Thickening
Published in Case Reports in Genetics (2025)Subjects: “…Biological Sciences…”
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Mitochondrial Dysfunction in Sickle Cell Trait Carriers With Exertional Collapse
Published in Case Reports in Genetics (2025)Subjects: “…Biological Sciences…”
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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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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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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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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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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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