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Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cells.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.61630
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- Publication type:
- Article
Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 2, p. 244, doi. 10.1002/ajmg.a.35632
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- Publication type:
- Article
Numerical aberrations of chromosome 1 in cervical intraepithelial neoplasia are strongly associated with infection with high-risk human papillomavirus types.
- Published in:
- Journal of Pathology, 2002, v. 198, n. 3, p. 300, doi. 10.1002/path.1222
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- Publication type:
- Article
Decreased expression of Ki-67 in atrophic cervical epithelium of post-menopausal women.
- Published in:
- Journal of Pathology, 2000, v. 190, n. 5, p. 545, doi. 10.1002/(SICI)1096-9896(200004)190:5<545::AID-PATH549>3.0.CO;2-S
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- Publication type:
- Article
LOSS OF CHROMOSOME 9 IN TISSUE SECTIONS OF TRANSITIONAL CELL CARCINOMAS AS DETECTED BY INTERPHASE CYTOGENETICS. A COMPARISON WITH RFLP ANALYSIS.
- Published in:
- Journal of Pathology, 1996, v. 179, n. 2, p. 169, doi. 10.1002/(SICI)1096-9896(199606)179:2<169::AID-PATH568>3.0.CO;2-J
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- Publication type:
- Article
DNA in situ hybridization as a diagnostic tool in the discrimination of melanoma and spitz naevus.
- Published in:
- Journal of Pathology, 1994, v. 173, n. 3, p. 227, doi. 10.1002/path.1711730305
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- Publication type:
- Article
Interphase cytogenetics of tumours.
- Published in:
- Journal of Pathology, 1992, v. 166, n. 3, p. 215, doi. 10.1002/path.1711660303
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- Publication type:
- Article
Long-term follow-up of type 1 lissencephaly: survival is related to neuroimaging abnormalities.
- Published in:
- 2011
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- Publication type:
- journal article
Structural and numerical changes of chromosome X in patients with esophageal atresia.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 9, p. 1077, doi. 10.1038/ejhg.2013.295
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- Publication type:
- Article
5q11.2 deletion in a patient with tracheal agenesis.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1265, doi. 10.1038/ejhg.2010.84
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- Publication type:
- Article
An Acute Promyelocytic Leukemia Resistant to All-Trans Retinoic Acid: A Case Report of the ZBTB16::RARa Variant and Review of the Literature.
- Published in:
- Case Reports in Oncology, 2023, v. 16, n. 1, p. 1443, doi. 10.1159/000534862
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- Publication type:
- Article
Genomic amplification of MYC as double minutes in a patient with APL-like leukemia.
- Published in:
- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0067-6
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- Publication type:
- Article
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with patient congenital anomalies.
- Published in:
- Molecular Cytogenetics (17558166), 2010, v. 3, p. 13, doi. 10.1186/1755-8166-3-13
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- Publication type:
- Article
Engineering large-scale chromosomal deletions by CRISPR-Cas9.
- Published in:
- Nucleic Acids Research, 2021, v. 49, n. 21, p. 12007, doi. 10.1093/nar/gkab557
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- Publication type:
- Article
Abnormalities of chromosome 1p/q are highly associated with chromosome 13/13q deletions and are an adverse prognostic factor for the outcome of high-dose chemotherapy in patients with multiple myeloma.
- Published in:
- British Journal of Haematology, 2007, v. 136, n. 4, p. 615, doi. 10.1111/j.1365-2141.2006.06481.x
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- Publication type:
- Article