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Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1...
Published 2025-01-01“…Molecular Genetics & Genomic Medicine…”
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82
A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy
Published 2025-01-01“…Molecular Genetics & Genomic Medicine…”
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83
Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection
Published 2025-01-01“…Molecular Genetics & Genomic Medicine…”
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84
A De Novo Frameshift Variant in SMC1A Causes Non‐Classic Cornelia de Lange Syndrome With Epilepsy: A Case Report and Literature Review
Published 2025-01-01“…Molecular Genetics & Genomic Medicine…”
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85
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype–Genotype Correlations From 175 Previous Cases and Identification of...
Published 2025-01-01“…Molecular Genetics & Genomic Medicine…”
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86
Carglumic acid as a treatment for persistent hyperammonemia in carnitine-acylcarnitine translocase deficiency: A case study
Published 2025-03-01“…Molecular Genetics and Metabolism Reports…”
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87
Inhibition of Glutamate‐to‐Glutathione Flux Promotes Tumor Antigen Presentation in Colorectal Cancer Cells
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88
A Novel P53-Related Activity in a Colon Adenocarcinoma Cell Line With Mutant P53
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89
Role of Transforming Growth Factor 1 in Lymphocyte Development and Death
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90
Allogeneic CD33-directed CAR-NKT cells for the treatment of bone marrow-resident myeloid malignancies
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Alginate Beads Encapsulated Auxin-Producing PGPR as a Biofertilizer Promotes Triticum aestivum Growth
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Genetic Variation of Lentil Landraces Across Different Altitudes in Azerbaijan
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A gene expression atlas of Nicotiana tabacum across various tissues at transcript resolution
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Intergenerational transport of double-stranded RNA in C. elegans can limit heritable epigenetic changes
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Intermediate MCAD Deficiency Associated with a Novel Mutation of the ACADM Gene: c.1052C>T
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