Found: 29
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Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia.
- Published in:
- International Journal of Hematology, 2014, v. 100, n. 6, p. 567, doi. 10.1007/s12185-014-1685-9
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- Article
Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
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- Orphanet Journal of Rare Diseases, 2007, v. 2, p. 9, doi. 10.1186/1750-1172-2-9
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- Publication type:
- Article
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 9, p. 1956, doi. 10.1002/ajmg.a.40355
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- Publication type:
- Article
Clinical Comparison of Overlapping Deletions of 19p13.3.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1110, doi. 10.1002/ajmg.a.35923
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- Publication type:
- Article
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 822, doi. 10.1002/ajmg.a.35699
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- Publication type:
- Article
Flow cytometric identification of cancer cells in effusions with Ca1 monoclonal antibody.
- Published in:
- 1985
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- Publication type:
- journal article
Ferritin-bearing lymphocytes in patients with cancer.
- Published in:
- 1984
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- Publication type:
- journal article
Phenotypes Associated with SHOX Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 12, p. 5674, doi. 10.1210/jcem.86.12.8125
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- Publication type:
- Article
Cytogenetic, morphologic and oncogene analysis of a cell line derived from a heterologous mixed mullerian tumor of the ovary.
- Published in:
- In Vitro Cellular & Developmental Biology Animal, 1997, v. 33, n. 5, p. 325, doi. 10.1007/s11626-997-0001-x
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- Publication type:
- Article
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
- Published in:
- Human Genetics, 2011, v. 130, n. 4, p. 517, doi. 10.1007/s00439-011-0970-4
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- Publication type:
- Article
Clinical significance and mechanisms associated with segmental UPD.
- Published in:
- Molecular Cytogenetics (17558166), 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13039-021-00555-0
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- Publication type:
- Article
Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms.
- Published in:
- Annals of Clinical & Laboratory Science, 2018, v. 48, n. 3, p. 264
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- Publication type:
- Article
Transformed aggressive γδ-variant T-cell large granular lymphocytic leukemia with acquired copy neutral loss of heterozygosity at 17q11.2q25.3 and additional aberrations.
- Published in:
- European Journal of Haematology, 2014, v. 93, n. 3, p. 260, doi. 10.1111/ejh.12313
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- Publication type:
- Article
Transformation of myeloma into Ph<sup>1</sup>-negative CML with plasma cell antigens.
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- American Journal of Hematology, 1985, v. 19, n. 3, p. 289, doi. 10.1002/ajh.2830190312
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- Publication type:
- Article
Trisomy D in Bone Marrow Cells in a Patient with Chronic Myelogenous Leukemia.
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- Acta Haematologica, 1974, v. 52, n. 1, p. 61, doi. 10.1159/000208221
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- Publication type:
- Article
Cellular immunity in patients with epidermoid cancer of the head and neck.
- Published in:
- Laryngoscope, 1979, v. 89, n. 4, p. 538, doi. 10.1288/00005537-197904000-00002
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- Publication type:
- Article
UPD detection using homozygosity profiling with a SNP genotyping microarray.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 4, p. 757, doi. 10.1002/ajmg.a.33939
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- Publication type:
- Article
An international standardization programme towards the application of gene expression profiling in routine leukaemia diagnostics: the Microarray Innovations in LEukemia study prephase.
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- British Journal of Haematology, 2008, v. 142, n. 5, p. 802, doi. 10.1111/j.1365-2141.2008.07261.x
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- Publication type:
- Article
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 5, p. 586, doi. 10.1002/pd.6554
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- Publication type:
- Article
Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy.
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- Prenatal Diagnosis, 2018, v. 38, n. 12, p. 920, doi. 10.1002/pd.5349
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- Publication type:
- Article
Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy.
- Published in:
- 2018
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- Publication type:
- journal article
The Role of c-MYC in B-Cell Lymphomas: Diagnostic and Molecular Aspects.
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- Genes, 2017, v. 8, n. 4, p. 116, doi. 10.3390/genes8040116
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- Publication type:
- Article
Intraventricular twin fetuses in fetu.
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- Journal of Neurosurgery, 2012, p. 17, doi. 10.3171/2011.10.PEDS11196
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- Publication type:
- Article
Burkitt Lymphoma Arising From Lymphoplasmacytic Lymphoma Following Acquisition of MYC Translocation and Loss of the ETV6 Tumor Suppressor Gene.
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- Archives of Pathology & Laboratory Medicine, 2013, v. 137, n. 1, p. 130, doi. 10.5858/arpa.2011-0429-CR
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- Publication type:
- Article
Four-Copy Number Intervals in SNP Microarray Analysis: Unique Patterns and Positions.
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- Cytogenetic & Genome Research, 2014, v. 144, n. 2, p. 92, doi. 10.1159/000368859
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- Publication type:
- Article
Cleft palate and complex chromosome rearrangements.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 3, p. 135, doi. 10.1111/j.1399-0004.1992.tb03225.x
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- Publication type:
- Article
Cell line segregation in a 45,X/46,XY mosaic child with asymmetric leg growth.
- Published in:
- Clinical Genetics, 1991, v. 40, n. 3, p. 237, doi. 10.1111/j.1399-0004.1991.tb03084.x
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- Publication type:
- Article
SPONTANEOUS REMISSION IN MONOSOMY 7 MYELODYSPLASTIC SYNDROME.
- Published in:
- British Journal of Haematology, 1995, v. 89, n. 4, p. 947, doi. 10.1111/j.1365-2141.1995.tb08449.x
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- Publication type:
- Article
Terminal transferase expression in acute myeloid leukaemia: biology and prognosis.
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- British Journal of Haematology, 1991, v. 78, n. 1, p. 48, doi. 10.1111/j.1365-2141.1991.tb04381.x
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- Publication type:
- Article