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Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 10, p. 629, doi. 10.1002/gcc.23070
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- Publication type:
- Article
Evidence that instability within the FRA3B region extends four megabases.
- Published in:
- Oncogene, 2002, v. 21, n. 57, p. 8713, doi. 10.1038/sj.onc.1205950
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- Publication type:
- Article
Cover Image.
- Published in:
- 2019
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- 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
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- Publication type:
- Article
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinoma.
- Published in:
- Oncogene, 2003, v. 22, n. 46, p. 7233, doi. 10.1038/sj.onc.1207006
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- Publication type:
- Article
Common fragile sites are preferential targets for HPV16 integrations in cervical tumors.
- Published in:
- Oncogene, 2003, v. 22, n. 8, p. 1225, doi. 10.1038/sj.onc.1206170
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- Publication type:
- Article
The genomic landscape of small intestine neuroendocrine tumors.
- Published in:
- 2013
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- Publication type:
- journal article
The genomic landscape of small intestine neuroendocrine tumors.
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 6, p. 2502, doi. 10.1172/JCI67963
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- Publication type:
- Article
American College of Medical Genetics Standards and Guidelines for Interpretation and Reporting of Postnatal Constitutional Copy Number Variants.
- Published in:
- Journal of International Reproductive Health/Family Planning, 2014, v. 33, n. 3, p. 217
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- Publication type:
- Article
The human factor IX gene as germline mutagen test: Samples from mainland China have the putatively endogenous pattern of mutation.
- Published in:
- Human Mutation, 2000, v. 16, n. 1, p. 31, doi. 10.1002/1098-1004(200007)16:1<31::AID-HUMU6>3.0.CO;2-I
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- Publication type:
- Article
Germline mutations in Peruvian patients with hemophilia B: Pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern.
- Published in:
- Human Mutation, 1998, v. 11, n. 5, p. 372, doi. 10.1002/(SICI)1098-1004(1998)11:5<372::AID-HUMU4>3.0.CO;2-M
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- 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
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- 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
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- Publication type:
- Article
Developmental delay and failure to thrive associated with a loss‐of‐function variant in WHSC1 (NSD2).
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2798, doi. 10.1002/ajmg.a.40498
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- 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
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- Publication type:
- Article
Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2152, doi. 10.1002/ajmg.a.35574
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- Publication type:
- Article