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[Related PubMed/MEDLINE]
Total Number of Papers: 20
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| No. |
Year |
Title |
Co-occurring Abbreviation |
| 1 |
2020 |
Genome-Wide Detection of CNVs and Association With Body Weight in Sheep Based on 600K SNP Arrays. |
CNVRs, CNVs |
| 2 |
2020 |
Wide-Angle Coronary Bifurcation Stenotic Lesions Treated With One Drug-Eluting Stent and Sequential Balloon Technique: A Better Strategy? |
BMS, DES, FKB, MACE, PCI, TLR |
| 3 |
2019 |
Evolution and functional divergence of MADS-box genes in Pyrus. |
TD, WGD |
| 4 |
2019 |
Genome-wide identification and characterization of R2R3-MYB genes in Medicago truncatula. |
qRT-PCR, TD |
| 5 |
2019 |
Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory. |
MLPA, NCBI, NGS |
| 6 |
2018 |
An Extended Targeted Copy Number Variation Detection Array Including 187 Genes for the Diagnostics of Neuromuscular Disorders. |
CGH-array, CNV, NEB, NM, NMDs, TPM3, TTN |
| 7 |
2017 |
Segmental duplications: evolution and impact among the current Lepidoptera genomes. |
SDs, TEs |
| 8 |
2017 |
The incidence and outcome of allied disorders of Hirschsprung's disease in Japan: Results from a nationwide survey. |
ADHD, CIIP, HG, IASA, MMIHS |
| 9 |
2016 |
Draft Genome of the Wheat Rust Pathogen (Puccinia triticina) Unravels Genome-Wide Structural Variations during Evolution. |
--- |
| 10 |
2013 |
Massive screening of copy number population-scale variation in Bos taurus genome. |
CNVs |
| 11 |
2012 |
Further clinical and molecular delineation of the 15q24 microdeletion syndrome. |
--- |
| 12 |
2012 |
Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation. |
AML, MDS |
| 13 |
2011 |
Copy number variation analysis in the great apes reveals species-specific patterns of structural variation. |
CNVs |
| 14 |
2011 |
Transcriptional variations mediated by an alternative promoter of the FPR3 gene. |
FPR3 |
| 15 |
2009 |
Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes. |
CNVs, GST, GSTT1, kb, LD |
| 16 |
2009 |
SNP discovery and haplotype analysis in the segmentally duplicated DRD5 coding region. |
--- |
| 17 |
2008 |
A highly conserved segmental duplication in the subtelomeres of Plasmodium falciparum chromosomes varies in copy number. |
FISH, qPCR |
| 18 |
2008 |
A shared promoter region suggests a common ancestor for the human VCX/Y, SPANX, and CSAG gene families and the murine CYPT family. |
CPL |
| 19 |
2003 |
[Segment duplications in the human genome]. |
--- |
| 20 |
1991 |
Visualization of myosin exchange between synthetic thick filaments. |
NHS-biotin, QD |
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