Found: 24
Select item for more details and to access through your institution.
Automated 3D scoring of fluorescence in situ hybridization (FISH) using a confocal whole slide imaging scanner.
- Published in:
- Applied Microscopy, 2021, v. 51, n. 1, p. 1, doi. 10.1186/s42649-021-00053-y
- By:
- Publication type:
- Article
A novel case of cutaneous myxoid spindle cell neoplasm with FMR1‐ALK gene fusion and CD34/S100 co‐expression.
- Published in:
- Journal of Cutaneous Pathology, 2023, v. 50, n. 6, p. 505, doi. 10.1111/cup.14354
- By:
- Publication type:
- Article
Neurological Manifestations of X-Linked Ichthyosis: Case Report and Review of the Literature.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13.
- Published in:
- Case Reports in Genetics, 2016, p. 1, doi. 10.1155/2016/7397405
- By:
- Publication type:
- Article
Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients.
- Published in:
- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01101-2
- By:
- Publication type:
- Article
CNKSR2 deletions: A novel cause of X-linked intellectual disability and seizures.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 7, p. 1668, doi. 10.1002/ajmg.a.36902
- By:
- Publication type:
- Article
Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2514, doi. 10.1002/ajmg.a.36663
- By:
- Publication type:
- Article
Rare and novel RUNX1 fusions in myeloid neoplasms: A single‐institute experience.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 2, p. 100, doi. 10.1002/gcc.22901
- By:
- Publication type:
- Article
Copy number variant analysis using genome‐wide mate‐pair sequencing.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 9, p. 459, doi. 10.1002/gcc.5
- By:
- Publication type:
- Article
Genetic and Epigenetic Changes in Chromosomally Stable and Unstable Progeny of Irradiated Cells.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107722
- By:
- Publication type:
- Article
Impact of RNA degradation on fusion detection by RNA-seq.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3161-9
- By:
- Publication type:
- Article
Highly sensitive single tube B‐lymphoblastic leukemia/lymphoma minimal/measurable residual disease test robust to surface antigen directed therapy.
- Published in:
- Cytometry. Part B, 2023, v. 104, n. 4, p. 279, doi. 10.1002/cyto.b.22120
- By:
- Publication type:
- Article
Cover Image.
- Published in:
- 2019
- By:
- Publication type:
- Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
- Published in:
- European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
- By:
- Publication type:
- Article
Genome Editing as a Tool toward Better Functional Understanding of Variants Identified by Next-Generation Sequencing.
- Published in:
- Clinical Chemistry, 2015, v. 61, n. 3, p. 564, doi. 10.1373/clinchem.2014.235663
- By:
- Publication type:
- Article
Prenatal Diagnosis of Chromosome Abnormalities: Past, Present, and Future.
- Published in:
- Clinical Chemistry, 2013, v. 59, n. 10, p. 1432, doi. 10.1373/clinchem.2013.204149
- By:
- Publication type:
- Article
Germ cell tumors and associated hematologic malignancies evolve from a common shared precursor.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Multilineage involvement in KMT2A‐rearranged B acute lymphoblastic leukaemia: cell‐of‐origin, biology, and clinical implications.
- Published in:
- Histopathology, 2024, v. 85, n. 2, p. 310, doi. 10.1111/his.15203
- By:
- Publication type:
- Article
The t(11;14)(q13;q32)/CCND1–IGH translocation in chronic lymphocytic leukaemia/small lymphocytic lymphoma: an unusual genetic aberration during the natural clinical course.
- Published in:
- Histopathology, 2019, v. 75, n. 2, p. 291, doi. 10.1111/his.13885
- By:
- Publication type:
- Article
Performance of MYC, BCL2, and BCL6 break-apart FISH in small biopsies with large B-cell lymphoma: a retrospective Cytopathology Hematopathology Interinstitutional Consortium study.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1408238
- By:
- Publication type:
- Article
Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide.
- Published in:
- Journal of Women's Health (15409996), 2017, v. 26, n. 7, p. 755, doi. 10.1089/jwh.2016.6098
- By:
- Publication type:
- Article
Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features.
- Published in:
- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0233-0
- By:
- Publication type:
- Article
Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3.
- Published in:
- Molecular Cytogenetics (17558166), 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8166-6-19
- By:
- Publication type:
- Article
Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome.
- Published in:
- 2021
- By:
- Publication type:
- journal article