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PLAG1 Immunohistochemical Staining Is a Surrogate Marker for PLAG1 Fusions in Lipoblastomas.
- Published in:
- Pediatric & Developmental Pathology, 2022, v. 25, n. 2, p. 134, doi. 10.1177/10935266211043366
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- Publication type:
- Article
Primary Knee Intra-articular Synovial Sarcoma in Pediatric and Adolescent Patients.
- Published in:
- Pediatric & Developmental Pathology, 2021, v. 24, n. 2, p. 159, doi. 10.1177/1093526620981368
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- Publication type:
- Article
MECP2 duplication: Possible cause of severe phenotype in females.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 4, p. 1029, doi. 10.1002/ajmg.a.36380
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- Publication type:
- Article
Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 gene.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1437, doi. 10.1002/ajmg.a.35342
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- Publication type:
- Article
Phenotype of FOXP2 haploinsufficiency in a mother and son.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 174, doi. 10.1002/ajmg.a.34354
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- Publication type:
- Article
Efficacy and safety of FLAG‐IDA as front‐line therapy in de novo paediatric acute myeloid leukaemia population.
- Published in:
- British Journal of Haematology, 2023, v. 202, n. 1, p. e3, doi. 10.1111/bjh.18844
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- Publication type:
- Article
A framework for the clinical implementation of optical genome mapping in hematologic malignancies.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 4, p. 642, doi. 10.1002/ajh.27175
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- Publication type:
- Article
Acute Myeloid Leukemia: The Challenge of Unfavorable Cytosenetics.
- Published in:
- Oncology (08909091), 2012, v. 26, n. 8, p. 724
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- Publication type:
- Article
Cytogenetics Is a Science, Not a Technique! Why Optical Genome Mapping Is So Important to Clinical Genetic Laboratories.
- Published in:
- 2023
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- Publication type:
- Editorial
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-29
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- Publication type:
- Article
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 455, doi. 10.1038/ejhg.2012.165
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- Publication type:
- Article
Expansion of the (CTG)n repeat in the 5′-UTR of a reporter gene impedes translation.
- Published in:
- Nucleic Acids Research, 2000, v. 28, n. 20, p. 3943, doi. 10.1093/nar/28.20.3943
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- Publication type:
- Article
RCSD1-ABL1 Translocation Associated with IKZF1 Gene Deletion in B-Cell Acute Lymphoblastic Leukemia.
- Published in:
- Case Reports in Hematology, 2015, p. 1, doi. 10.1155/2015/353247
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- Publication type:
- Article
A Unique ''Composite'' PTLD with Diffuse Large B-Cell and T/Anaplastic Large Cell Lymphoma Components Occurring 17 Years after Transplant.
- Published in:
- Case Reports in Hematology, 2013, p. 1, doi. 10.1155/2013/386147
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- Publication type:
- Article
Development of second genetically distinct T‐lymphoblastic leukemia in a pediatric patient.
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 8, p. 1, doi. 10.1002/pbc.31050
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- Publication type:
- Article
IKZF1<sup>PLUS</sup> alterations contribute to outcome disparities in Hispanic/Latino children with B‐lymphoblastic leukemia.
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 7, p. 1, doi. 10.1002/pbc.30996
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- Publication type:
- Article
Myeloid lineage switch following chimeric antigen receptor T-cell therapy in a patient with TCF3-ZNF384 fusion-positive B-lymphoblastic leukemia.
- Published in:
- 2018
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- Publication type:
- journal article
Segmental Chromosomal Aberrations in Localized Neuroblastoma Can be Detected in Formalin-Fixed Paraffin-Embedded Tissue Samples and Are Associated With Recurrence.
- Published in:
- 2016
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- Publication type:
- journal article
Analytic Validation of Optical Genome Mapping in Hematological Malignancies.
- Published in:
- Biomedicines, 2023, v. 11, n. 12, p. 3263, doi. 10.3390/biomedicines11123263
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- Publication type:
- Article
MLL Rearrangment and EVI1 Deletion in BCR/ABL1 Positive Chronic Myeloid Leukemia.
- Published in:
- 2013
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- Publication type:
- Case Study
Two cases of localized neuroblastoma with multiple segmental chromosomal alterations and metastatic progression.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 2, p. 332, doi. 10.1002/pbc.24311
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- Publication type:
- Article
Pediatric Metastatic Hepatoblastoma With an ARID1A Mutation and Rhabdoid Cells.
- Published in:
- International Journal of Surgical Pathology, 2022, v. 30, n. 3, p. 307, doi. 10.1177/10668969211042638
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- Publication type:
- Article
Primary Adrenal Malignant Rhabdoid Tumor in a 14-Year-Old Female: A Case Report and Literature Review.
- Published in:
- International Journal of Surgical Pathology, 2022, v. 30, n. 2, p. 172, doi. 10.1177/10668969211024331
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- Publication type:
- Article
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community‐driven standards.
- Published in:
- Human Mutation, 2018, v. 39, n. 11, p. 1721, doi. 10.1002/humu.23651
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- Publication type:
- Article
MYC Amplification in Angiosarcoma Arising from an Arteriovenous Graft Site.
- Published in:
- Case Reports in Pathology, 2015, p. 1, doi. 10.1155/2015/537297
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- Publication type:
- Article
MYC Amplification in Angiosarcoma Arising from an Arteriovenous Graft Site.
- Published in:
- Case Reports in Pathology, 2015, p. 1, doi. 10.1155/2015/537297
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- Publication type:
- Article
Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2021, v. 145, n. 2, p. 176, doi. 10.5858/arpa.2020-0089-CP
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- Publication type:
- Article
Standard operating procedure for curation and clinical interpretation of variants in cancer.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0687-x
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- Publication type:
- Article