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Exome sequencing
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publication
Lessons from whole-exome sequencing in MODYX families
2014 |
2. lékařská fakulta
publication
NFKB2 Mutation Diagnosed by Whole Exome Sequencing (WES) in a Patient with Complex Phenotype and Hypogammaglobulinemia
2019 |
2. lékařská fakulta
publication
Whole Exome Sequencing of Epithelial Ovarian Carcinomas Differing in Resistance to Platinum Therapy
2022 |
1. lékařská fakulta, 2. lékařská fakulta, Lékařská fakulta v Plzni, 3. lékařská fakulta
publication
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
Publikace bez příslušnosti k fakultě
publication
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
2024 |
2. lékařská fakulta
publication
Predictors of whole exome sequencing in dystonic cerebral palsy and cerebral palsy-like disorders
2023 |
1. lékařská fakulta
publication
Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease
2023 |
1. lékařská fakulta, 2. lékařská fakulta, Ústřední knihovna, 3. lékařská fakulta
publication
Yield of exome sequencing in patients with developmental and epileptic encephalopathies and inconclusive targeted gene panel
2024 |
2. lékařská fakulta
publication
Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer
2022 |
Lékařská fakulta v Plzni
publication
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant
2022 |
2. lékařská fakulta
publication
Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer
2021 |
Lékařská fakulta v Plzni
publication
Diagnostic Utility of Exome Sequencing for Kidney Disease
2019 |
1. lékařská fakulta
publication
A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio-based exome sequencing: A case report
2023 |
2. lékařská fakulta
publication
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing
2012 |
1. lékařská fakulta
publication
Whole-Exome Sequencing in Czech Patients with Neurogenetic Diseases
2020 |
2. lékařská fakulta
publication
Exome sequencing for identification of disease genes for rare syndromes. Experiences from Hamburg
2014 |
2. lékařská fakulta
publication
Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing
2017 |
1. lékařská fakulta
publication
Whole Exome Sequencing Analysis of ABCC8 and ABCD2 Genes Associating With Clinical Course of Breast Carcinoma
2015 |
1. lékařská fakulta, Lékařská fakulta v Plzni
publication
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
2020 |
2. lékařská fakulta
publication
Clinically relevant copy-number variants in exome sequencing data of patients with dystonia
2021 |
1. lékařská fakulta
publication
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals
2021 |
Ústřední knihovna
publication
Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer
2022 |
Lékařská fakulta v Plzni
publication
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
2019 |
2. lékařská fakulta
publication
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia
2019 |
2. lékařská fakulta
publication
Whole Exome Sequencing of Aberrant Plasma Cells in a Patient with Multiple Myeloma Minimal Residual Disease
2017 |
Publikace bez příslušnosti k fakultě
publication
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis
2021 |
2. lékařská fakulta
publication
Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
2015 |
1. lékařská fakulta
publication
Exome Sequencing of Paired Colorectal Carcinomas and Synchronous Liver Metastases for Prognosis and Therapy Prediction
2023 |
1. lékařská fakulta, Lékařská fakulta v Plzni
publication
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease
2018 |
1. lékařská fakulta
publication
Prognostic potential of whole exome sequencing in the clinical management of metachronous colorectal cancer liver metastases
2023 |
Lékařská fakulta v Plzni