Found: 26
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Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection: a case report.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Oligonucleotide Array for Mutation Analysis in Familial Breast Cancer.
- Published in:
- 1999
- By:
- Publication type:
- Abstract
Unravelling Genetic Data by Arrayed Primer Extension.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2000, v. 38, n. 2, p. 165
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- Publication type:
- Article
Universal and flexible DNA microarray approach: arrayed primer extension.
- Published in:
- 1999
- By:
- Publication type:
- Abstract
Methylation Markers of Early-Stage Non-Small Cell Lung Cancer.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039813
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- Publication type:
- Article
The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General Population.
- Published in:
- Cancers, 2023, v. 15, n. 14, p. 3663, doi. 10.3390/cancers15143663
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- Publication type:
- Article
Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 2, p. 162, doi. 10.1038/sj.ejhg.5201738
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- Publication type:
- Article
Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0444-2
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- Publication type:
- Article
Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics.
- Published in:
- Endocrinology, 2019, v. 160, n. 7, p. 1731, doi. 10.1210/en.2019-00165
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- Publication type:
- Article
Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.
- Published in:
- Clinical Rheumatology, 2021, v. 40, n. 10, p. 4157, doi. 10.1007/s10067-021-05756-x
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- Publication type:
- Article
Implementation of Risk-Stratified Breast Cancer Prevention With a Polygenic Risk Score Test in Clinical Practice.
- Published in:
- Breast Cancer: Basic & Clinical Research, 2023, p. 1, doi. 10.1177/11782234231205700
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- Publication type:
- Article
DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns.
- Published in:
- Genome Biology, 2014, v. 15, n. 4, p. R54, doi. 10.1186/gb-2014-15-4-r54
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- Publication type:
- Article
Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual.
- Published in:
- Current Genetics, 2014, v. 60, n. 1, p. 11, doi. 10.1007/s00294-013-0398-6
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- Publication type:
- Article
A first-generation linkage disequilibrium map of human chromosome 22.
- Published in:
- Nature, 2002, v. 418, n. 6897, p. 544, doi. 10.1038/nature00864
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- Publication type:
- Article
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.
- Published in:
- International Journal of Cancer, 2018, v. 142, n. 3, p. 540, doi. 10.1002/ijc.31076
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- Publication type:
- Article
Correction: Methylation Markers of Early-Stage Non-Small Cell Lung Cancer.
- Published in:
- 2017
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- Publication type:
- Correction Notice
Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 10, p. 812, doi. 10.1002/gcc.20902
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- Publication type:
- Article
From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.936131
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- Publication type:
- Article
Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting.
- Published in:
- Prenatal Diagnosis, 2019, v. 39, n. 13, p. 1262, doi. 10.1002/pd.5578
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- Publication type:
- Article
Molecular diagnosis of Down syndrome using quantitative APEX-2 microarrays.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 12/13, p. 1170, doi. 10.1002/pd.2639
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- Publication type:
- Article
Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans.
- Published in:
- Human Mutation, 2011, v. 32, n. 7, p. 806, doi. 10.1002/humu.21508
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- Publication type:
- Article
Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1916-3
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- Publication type:
- Article
Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 15, doi. 10.1186/1471-2350-11-15
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- Publication type:
- Article