Found: 19
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Bipolar affective disorders linked to DNA markers on chromosome 11.
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- Nature, 1987, v. 325, n. 6107, p. 783, doi. 10.1038/325783a0
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- Article
Evidence against Ha-ras-1 involvement in sporadic and familial melanoma.
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- Nature, 1987, v. 325, n. 6099, p. 73, doi. 10.1038/325073a0
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- Article
CTD<sup>2</sup> Dashboard: a searchable web interface to connect validated results from the Cancer Target Discovery and Development Network.
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- Database: The Journal of Biological Databases & Curation, 2017, v. 2017, n. 1, p. 1, doi. 10.1093/database/bax054
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- Article
International network of cancer genome projects.
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- Nature, 2010, v. 464, n. 7291, p. 993, doi. 10.1038/nature08987
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- Article
Replicating genotype–phenotype associations.
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- Nature, 2007, v. 447, n. 7145, p. 655, doi. 10.1038/447655a
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- Article
SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.
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- Nucleic Acids Research, 2006, v. 34, n. suppl 1, p. d617, doi. 10.1093/nar/gkj151
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- Article
Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer.
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- International Journal of Cancer, 2007, v. 121, n. 11, p. 2532, doi. 10.1002/ijc.22985
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- Article
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.
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- Nature Communications, 2015, v. 6, n. 12, p. 10013, doi. 10.1038/ncomms10013
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- Article
Human Uteroglobin Gene: Structure, Subchromosomal Localization, and Polymorphism.
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- DNA & Cell Biology, 1997, v. 16, n. 1, p. 73, doi. 10.1089/dna.1997.16.73
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- Article
Fine mapping and evaluation of candidate genes for cervical cancer on 11q23.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 1, p. 95, doi. 10.1002/gcc.20151
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- Article
Cervical cancer suppressor gene is within 1 cM on 6p23.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 4, p. 373, doi. 10.1002/(SICI)1098-2264(200004)27:4<373::AID-GCC6>3.0.CO;2-V
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- Article
Cervial intraepithelial neoplasia III shows frequent allelic loss in 3p and 6p.
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- Genes, Chromosomes & Cancer, 1998, v. 22, n. 1, p. 57, doi. 10.1002/(SICI)1098-2264(199805)22:1<57::AID-GCC8>3.0.CO;2-6
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- Article
A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group study.
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- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208936
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- Article
Description of amish study data set.
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- Genetic Epidemiology, 1989, v. 6, n. 1, p. 195, doi. 10.1002/gepi.1370060135
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- Article
Novel mutations of APOB cause apoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
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- Human Mutation, 2002, v. 20, n. 5, p. 402, doi. 10.1002/humu.10135
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- Article
Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
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- Human Mutation, 2002, v. 20, n. 2, p. 110, doi. 10.1002/humu.10101
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- Article
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
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- JNCI: Journal of the National Cancer Institute, 2024, v. 116, n. 1, p. 149, doi. 10.1093/jnci/djad183
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- Article
Localization of a Tumor Suppressor Gene in 11p15.5 Using the G401 Wilms' Tumor Assay.
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- Human Molecular Genetics, 1996, v. 5, n. 2, p. 239, doi. 10.1093/hmg/5.2.239
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- Article
Framework for quality assessment of whole genome cancer sequences.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18688-y
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- Article