277 results on '"Cooley, Linda"'
Search Results
2. Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours
3. Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
4. T-lymphoblastic leukemia/lymphoma with interfollicular growth pattern and Castleman-like morphologic features
5. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders
6. Maintaining a methods database to optimize solid tumor tissue culture: Review of a 15-year database from a single institution
7. The Role of Communication in Strategic Planning at California Community Colleges
8. Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC)
9. Using Study Guides: An Approach to Self-Access.
10. Clinical Cytogenetics and Testing for Developmental Disabilities
11. Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biological Features
12. The Cytogenetics of Solid Tumors
13. eP419: Genotype-phenotype correlation of distal 18q deletions less than 5 Mb
14. 1. Clinicopathologic analysis of gliomas harboring ROS1 gene arrangements
15. Dissertation Writing in Action: The Development of a Dissertation Writing Support Program for ESL Graduate Research Students.
16. Oral Needs and Difficulties of Graduate Students in Hong Kong.
17. Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing
18. Many clinical laboratories performing next-generation sequencing have no future plans to migrate to GRCh38
19. 2. Giant cell glioblastoma with massive loss of heterozygosity: A new molecularly defined subtype
20. Guidance for Fluorescence in Situ Hybridization Testing in Hematologic Disorders
21. Prognostic significance of cytogenetically detected chromosome 21 anomalies in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study
22. HER-2 fluorescence in situ hybridization: results from the survey program of the College of American Pathologists
23. Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus Assay
24. Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastoma
25. The Cytogenetics of Solid Tumors
26. Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes
27. Contributors
28. Conventional and Molecular Cytogenetics of Neoplasia
29. Cuplike nuclear morphology is highly associated with IKZF1 deletion in pediatric precursor B-cell ALL
30. Higher dose imatinib for children with de novo chronic phase chronic myelogenous leukemia: A report from the Childrenʼs Oncology Group
31. 7. ROS1-GOPC gene fusion characterizes a minor subset of brain tumors
32. 63. Near-haploidization molecularly defines giant cell glioblastoma
33. 20. A resource for our clinical genomics community: The Compendium of Cancer Genome Aberrations (CCGA)
34. Application of 2016 WHO classification in the diagnosis of paediatric high-grade MYC-negative mature B-cell lymphoma with Burkitt-like morphological features
35. Occurrence and characterization of medulloblastoma in a patient with Curry‐Jones syndrome
36. An interstitial 15q11-q14 deletion: Expanded Prader-Willi syndrome phenotype
37. Autistic and dysmorphic features associated with a submicroscopic 2q33.3–q34 interstitial deletion detected by array comparative genomic hybridization
38. Juxtaglomerular cell tumor in an 8-year-old girl
39. Infant with Granulocytic Sarcoma of the Ovary: An Unusual Case Presentation of Acute Myelogenous Leukemia (M6)
40. 27. ACMG/CGC technical laboratory standards for interpretation and reporting of acquired copy number abnormalities (CNAs) and copy-neutral loss of heterozygosity (CN-LOH) in neoplastic disorders
41. Cytogenetic heteromorphisms: survey results and reporting practices of Giemsa-band regions that we have pondered for years
42. Application of 2016 WHO classification in the diagnosis of paediatric high-grade MYC-negative mature B-cell lymphoma with Burkitt-like morphological features.
43. 5. Progress and future of the compendium of Cancer Genome Aberrations (CCGA)
44. 41. Impact of chromosome aberrations on tumor recurrence risk in grade I–II pilocytic astrocytoma
45. Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformations
46. Juvenile myelomonocytic leukemia with t(3;5)(q25;q35), Auer rods and marked myelodysplasia
47. Dissertation Writing in Practice : Turning Ideas into Text
48. Full Disclosure
49. Imidazole as a pH probe: An NMR experiment for the general chemistry laboratory
50. Clear cell sarcoma of tendons and aponeuroses: a review
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.