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Identifying Contact Time Required for Secondary Transmission of Clostridioides difficile Infections by Using Real-Time Locating System.
- Published in:
- Emerging Infectious Diseases, 2024, v. 30, n. 5, p. 908, doi. 10.3201/eid3005.231588
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- Article
Comparative Analysis of the Molecular Characteristics of Group B Streptococcus Isolates Collected from Pregnant Korean Women Using Whole-genome Sequencing.
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- Annals of Laboratory Medicine, 2023, v. 43, n. 2, p. 180, doi. 10.3343/alm.2023.43.2.180
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- Article
Adult-onset MELAS syndrome in a 51-year-old woman without typical clinical manifestations: a case report.
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- European Heart Journal Case Reports, 2023, v. 7, n. 1, p. 1, doi. 10.1093/ehjcr/ytad028
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- Article
Clinical Characteristics and Audiological Profiles of Patients with Pathogenic Variants of WFS1.
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- Journal of Clinical Medicine, 2024, v. 13, n. 16, p. 4851, doi. 10.3390/jcm13164851
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- Article
Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.
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- Journal of Clinical Medicine, 2024, v. 13, n. 7, p. 2001, doi. 10.3390/jcm13072001
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- Publication type:
- Article
Prevalence Estimation of the PALB2 Germline Variant in East Asians and Koreans through Population Database Analysis.
- Published in:
- Cancers, 2024, v. 16, n. 19, p. 3318, doi. 10.3390/cancers16193318
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- Article
Circulating Tumor DNA Analysis on Metastatic Prostate Cancer with Disease Progression.
- Published in:
- Cancers, 2023, v. 15, n. 15, p. 3998, doi. 10.3390/cancers15153998
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- Publication type:
- Article
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1178582
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- Publication type:
- Article
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1178582
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- Publication type:
- Article
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy.
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- Epilepsia (Series 4), 2024, v. 65, n. 3, p. 766, doi. 10.1111/epi.17857
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- Publication type:
- Article
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.978532
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- Publication type:
- Article
Copy‐number analysis by base‐level normalization: An intuitive visualization tool for evaluating copy number variations.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 1, p. 35, doi. 10.1111/cge.14236
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- Publication type:
- Article
In Silico identification of a common mobile element insertion in exon 4 of RP1.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-92834-4
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- Article
Clinical accuracy and utility of plasma microbial cell free DNA whole genome sequencing in the diagnosis of invasive aspergillosis in patients with hematologic malignancies or coronavirus disease.
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- Infection & Chemotherapy, 2022, v. 54, p. 281
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- Publication type:
- Article
Reanalysis of Genomic Sequencing Results in a Clinical Laboratory: Advantages and Limitations.
- Published in:
- Frontiers in Neurology, 2020, p. 1, doi. 10.3389/fneur.2020.00612
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- Publication type:
- Article
Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposis.
- Published in:
- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0553-0
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- Publication type:
- Article
Histopathologic image–based deep learning classifier for predicting platinum-based treatment responses in high-grade serous ovarian cancer.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48667-6
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- Publication type:
- Article
Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort.
- Published in:
- Genes, 2022, v. 13, n. 1, p. 27, doi. 10.3390/genes13010027
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- Publication type:
- Article
TUBB3 M323V Syndrome Presents with Infantile Nystagmus.
- Published in:
- Genes, 2021, v. 12, n. 4, p. 575, doi. 10.3390/genes12040575
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- Publication type:
- Article
Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy.
- Published in:
- PLoS ONE, 2019, v. 14, n. 6, p. 1, doi. 10.1371/journal.pone.0217521
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- Publication type:
- Article
Utility of Plasma Microbial Cell-Free DNA Whole-Genome Sequencing for Diagnosis of Invasive Aspergillosis in Patients With Hematologic Malignancy or COVID-19.
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- Journal of Infectious Diseases, 2023, v. 228, n. 4, p. 444, doi. 10.1093/infdis/jiad213
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- Publication type:
- Article
Comparison of High-Throughput Fully Automated Immunoanalyzers for Detecting Hepatitis B Virus Infection.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2020, v. 144, n. 5, p. 612, doi. 10.5858/arpa.2019-0096-OA
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- Article
Trajectory of genetic alterations associated with colistin resistance in Acinetobacter baumannii during an in-hospital outbreak of infection.
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- 2022
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- Publication type:
- journal article
Detection of minimal residual disease using circulating tumor DNA in patients treated with long-term PARP inhibitors maintenance for epithelial ovarian cancer.
- Published in:
- Journal of Gynecologic Oncology, 2024, v. 35, p. 22, doi. 10.3802/jgo.2024.35.S2.P4
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- Publication type:
- Article