28 results on '"Li, Marilyn M"'
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2. Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers.
3. Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
4. Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1Fusion in an Infant: A New Type of “Plagoma”
5. Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways.
6. Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
7. Cancer Predisposition Genetic Testing Among Children with Hematologic Malignancies
8. Development and Clinical Validation of a Large Fusion Gene Panel for Pediatric Cancers
9. The spectrum of RAF1 fusion positive solid tumors in children and young adults.
10. Pediatric-Specific Patterns of Clonal Evolution Arising from Acquired Aplastic Anemia
11. Pediatric-Specific Patterns of Clonal Evolution Arising from Acquired Aplastic Anemia
12. Overgrowth Syndromes Caused by Somatic Variants in the Phosphatidylinositol 3-Kinase/AKT/Mammalian Target of Rapamycin Pathway
13. Molecular Diagnosis of Mosaic Overgrowth Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
14. Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer
15. Alternative splicing of its 5’-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies
16. Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine.
17. American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders
18. Common Leukemia- and Lymphoma-Associated Genetic Aberrations in Healthy Individuals
19. Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation
20. Assessments of Somatic Variant Classification Using the AMP/ASCO/CAP Guidelines: A Report from the Association for Molecular Pathology
21. A Novel FBXO45-Gef-H1 Axis Controls Oncogenic Signaling in B-Cell Lymphoma
22. A Novel FBXO45-Gef-H1 Axis Controls Oncogenic Signaling in B-Cell Lymphoma
23. Characterization of a cryptic 3.3 Mb deletion in a patient with a “balanced t(15;22) translocation” using high density oligo array CGH and gene expression arraysHow to cite this article: Li MM, Nimmakayalu MA, Mercer D, Andersson HC, Emanuel BS. 2008. Characterization of a cryptic 3.3 Mb deletion in a patient with a “balanced t(15;22) translocation” using high density oligo array CGH and gene expression arrays. Am J Med Genet Part A 146A:368–375.
24. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis
25. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis
26. Leadership and management in pediatric emergency medicine
27. Technical Standards and Guidelines for Use of Clinical Genomic Microarray Analysis in Hematopoietic and Other Neoplastic Disorders: A Draft From a Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee
28. Technical Standards and Guidelines for Use of Clinical Genomic Microarray Analysis in Hematopoietic and Other Neoplastic Disorders: A Draft From a Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee
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